Related Post

Blog Archive

information about stem cells

information about stem cells

shall we have a look at your baby? - you're 27 weeks now, aren't you?- yeah.- okay. oh, that's a nice one, isn't it?that's always good, isn't it? birth defects represent one of the major causes of morbidity and mortality in children. there's about three in every 100 babies

which are born with a major birth defect. we are faced many times with a situation in which we don't know what to do for these babies. - it's a girl.- it's a girl. i collaborate with paolo de coppi.i look after the mums while they're pregnant. paolo visits the fetal medicine unit,and he sees the mums if the baby has an abnormality because he looks after the babywhen they're born. and we're trying to develop

treatments using stem cellsin the amniotic fluid around the baby. stem cells have represented a major breakthrough because it's the possibility of growing cellsoutside the body to make a repair to the children once the cells have been built in the laboratory. so what we have developed in the last few years and this has been initially the work we have done

with antony atala at the wake forest institute of regenerative medicine and is the possibility of deriving stem cell from the amniotic fluid. these are not embryonic stem cells but are neither adult stem cells. they have characteristics that are in between the two cell types, and for that, they present a bigadvantage for therapy. these cells would represent an ideal source

for building organ and tissue that are missing in the foetus. and this is because we can predict and diagnose very accurately these diseases before the foetus is born. once this diagnosis is made, however, we have about 20 weeks of gestation in which we can plan the engineered organ to be built outside of the baby,

that then can be eventually implanted once the baby is born. so we can correct that defect at birth using his own cells. here is where we do receive the samples from anna's. once the cells are isolated from the amniotic fluid,they can be easily expanded in this incubator

and eventually engineered in a three-dimensional structurethat can mimic the organs that the baby is missing. these organs can be expanded and grown in these bioreactors. we haven't got any treatments that will actually work yet. but we're working on this whole area. for instance, the mum that we scanned earlier onhas got a completely healthy, normal baby as far as i can tell on the scan. we're not looking to treat anybody right now.but we are trying to develop new

treatments which will improve already existing treatmentsor to develop completely new therapies, using the stem cells that are in the amniotic fluid. another situation in which we can intervene even before birth - we can use the same cells to treat the foetus. so if we know that the foetus has some malformation that can be corrected before birth,

we can use his own cells to, for treatment. so we can culture his or her cells outside the womb and expand them and eventually correct, for example, the gene that is altered or missing, using gene therapy technique. and we can inject back the cells

into the foetus before birth. and so somehow improving his option of life

induced pluripotent stem cells

induced pluripotent stem cells

this video will show you how to coat cultureplates with vitronectin, so you will be ready to transfer newly forming ipsc colonies orfrozen cultures to essential 8â„¢ medium. before using the essential 8â„¢ complete medium,you'll need to prepare vitronectin-coated plates. the optimal working concentrationof vitronectin is cell-line dependent and must be determined empirically. we recommendedusing a final coating concentration of 0.1–1.0 âµg/cm2 on the culture surface, dependingon your cell line. we routinely use vitronectin at 0.5 âµg/cm2 for human psc culture. prior to coating culture vessels, calculatethe working concentration of vitronectin using the following formula and dilute the stockappropriately. the product manual for vitronectin

contains a list of culture dish surface areasand volume of vitronectin required. as an example,, to coat a 6-well plate at a coatingconcentration of 0.5 âµg/cm2, you’ll need to prepare 6 ml of diluted vitronectin solution(10 cm2/well surface area and 1 ml of diluted vitronectin/well). upon receipt, thaw the vial of vitronectinat room temperature and prepare 60âµl aliquots of vitronectin in polypropylene tubes. freezethe aliquots at –80â°c or use immediately. to coat the wells of a 6-well plate, removea 60âµl aliquot of vitronectin from –80â°c storage and thaw at room temperature. you’llneed one 60âµl aliquot per 6-well plate. add 60 âµl of thawed vitronectin into a 50-mlconical tube containing 6 ml of sterile dpbs

without calcium and magnesium at room temperature.gently re-suspend by pipetting the vitronectin dilution up and down. this results in a working concentration of5 âµg/ml, a 1:100 dilution add 1 ml of the diluted vitronectin solutionto each well of a 6-well plate. when used to coat a 6-well plate (10 cm2/well) at 1ml/well, the final concentration will be 0.5 âµg/cm2. if you’re using a different type of culturevessel, refer to the vitronectin product insert for detailed information on volumes. incubate the coated plates at room temperaturefor 1 hour.

note: the culture vessel can now be used orstored at 2–8â°c wrapped in laboratory film for up to one week. do not allow the vesselto dry. prior to use, pre-warm the culture vessel to room temperature for at least 1hour.

human stem cells

human stem cells

an international team of researchers has developedan artificial version of the human midbrain using stem cells. the team's creation will allow for more extensiveresearch and drug testing,... and could have broad treatment implications -- especiallyfor degenerative disorders involving the motor system. park jong-hong explains. the breakthrough could eventually be life-alteringnews for patients of parkinson's disease. the leading degenerative disorder of the centralnervous system is a condition stemming from the midbrain, which is in charge of motorfunctions that control auditory and eye movements,

vision and body movements. the midbrain contains special neurons thatproduce dopamine, and the disease develops when the number of neurons decreases. with the breakthrough, scientists have createda miniature version of the midbrain, which they hope will shed light on exactly how parkinson'sevolves and lead to a cure for it and other aging-related brain diseases. while miniature versions of the brain havebeen developed before, this one is the first of its kind. it is a three-dimensional miniature with tissuesthat were grown in a laboratory using stem

cells cultivated from human blood, and itcan be used in a variety of drug tests instead of in experiments on actual patients. the medical community is abuzz about the possibilitiesfor research and treatment the breakthrough will have. the joint study was conducted by an internationalteam led by professor shawn je from duke-nus medical school and a*star's genome instituteof singapore. their findings were published this month inthe journal cell stem cell. park jong-hong arirang news.

human mesenchymal stem cells

human mesenchymal stem cells

- [voiceover] so, let megive you an analogy, here. when you were still anadorable little baby, you were just bursting with potential. you could decide to be a pilot, or a doctor, or a journalist. you had the potential to specialize into all sorts of different careers, and as you got a bit older,you got more and more committed down a certain pathway,

and the decisions that you made moved you further and furtheralong this pathway, right? well, it turns out that stemcells operate in a similar way, going from unspecializedto more specialized as they get older. so, let me show you what i mean by that over the course of this video. and let's actually startback at the zygote, here, the cell that resultswhen sperm and egg fuse

because that's really where our stem cell story kinda begins. so, the zygote starts to divide, right, by mitosis until it reachesthe blastocyst stage, this hollow ball of cellshere is called a blastocyst. and here, things start to geta little bit more interesting. so, in a blastocyst, there'sthis little grouping of cells down in here, referred toas the inner cell mass. and this is a really speciallittle bunch of cells

that go on to become the embryo. so, these are called stem cells. and what they can do as stem cells is they can specialize intoseveral other cell types. so, we actually call thempluripotent stem cells. pluri meaning several and potent referring to these stem cells' ability to actually do this differentiation. so, during development,these inner cell mass

pluripotent stem cells can differentiate into any of the more than200 different cell types in the adult human body whengiven the proper stimulation. so, it's kind of incredible to think that every single cell in your body can trace its ancestry back to this little group of stem cells, here. and actually, if you ever hear anyone talking about embryonic stem cells,

these are the ones they're referring to, these icm stem cells. so, is this the only placewe can find stem cells, here in the developmental structures? we used to think so, but, it turns out that in mammals, there aretwo main types of stem cells. embryonic stem cells that we just saw and somatic stem cells whichare found in every person. so, the embryonic stem cellsare used to build our bodies,

to go from one cell totrillions of specialized cells, and the somatic stem cells are used as sort of a repair system for the body, replenishing tissuesthat need to be replaced. and they can't repair everything, but, there's a lot of every day repairs that can happen because of our stem cells. so, in skin, for example... this outside layer is the partof our skin that we can see

and that we can touch, right? and it's made of these waterproof, pretty rugged epithelialor skin cells and interestingly, althoughthey are pretty rugged, you're constantlyshedding these skin cells. they actually just sort offall off or get rubbed off during every day activities like when you're putting your clothes on. and then, the ones from underneath them

just sort of move up and take their place. so, you shed them and you lose almost 40,000 of them per hour. so, if we wanna have anyhope of keeping our skin, we kinda need a way toreplace these cells, and that's where stem cells that live in our skin come in. actually, our skin cells are shed and replaced so often,that it only takes a month

for us to have a completely new skin. like, literally onemonth, entirely new skin. it's outrageous. anyway, deep within our skin, there's this layer of stem cells called epidermal stem cells, and their job is to becontinually dividing. so, you can see themdividing, here, dividing, dividing, dividing, and makingnew skin cells that go on

to migrate upward as themultiple layers of our skin. and their goal is to eventually replace these ones up here on the outside that get damaged or worn out and fall off. so, it's this kind of activity here which show off our stem cells' role as our regenerative cells. now, lemme just highlighta few differences between our mature skin cells over here

and our stem cells down here. they are very different. mature cells are notthe same as stem cells, and this principle goesfor really any mature cell versus any stem cell. so, the mature cell isalready specialized, it already has a really specific function. for example, our outer layerof epithelial cells, here, they have a protective function

against the outside environment. and, you know, just thinkingof other adult cell types, right, like muscle cellshave a contractile function, and neurons have amessage sending function, and bones have a rigidstructural function. so, all these adult cells are already nice and specialized, they'vegrown up and decided what they wanna do for a living, whereas, stem cells arenot like that at all.

stem cells are unspecialized. but, they still have areally important job, which is to give rise to ourmore specialized cell types, like these cells here, okay? and, actually, in order tobe considered a stem cell, and this goes for theembryonic stem cells we met previously and the somaticstem cells we're meeting now, to be a stem cell, you'd need to possess two main properties.

the ability to self renew,meaning you can divide and divide, and divide, but, at least one of your resultingcells remains a stem cell, it remains undifferentiated, and you'd need to have a high capacity to differentiate intomore specialized cells when the time comes. so, remember, this is also referred to as having some degree of potency.

and there's actually a few different types of stem cells, and someof them can turn into more types of cells than others. some are more potent than others. so, this epithelial stem cell we saw here is actually one of the lesspotent types of stem cell. in other words, thesestem cells can only divide and specialize into more epithelial cells. so, they're our source ofepithelial cells, sure,

but, only epithelial cellsand not any other cell type. so, we call them unipotent,referring to their ability to only create one type of cell. but, lemme show you another example here of a multipotent stem cell. let's look at this guy'sfemur, his thigh bone, which is where our blood cells are made inside bone marrow in our bones. so, you might know thatour red blood cells

have a life span of about four months. so, that means that we needto be constantly replacing our red blood cells orwe'll run out, right? well, in our bone marrow,we have what are called hematopoietic stem cells, which are our blood making stem cells. and these are pretty special, they're multipotent stem cells, which means they can giverise to many types of cells,

but, only ones within a specific family. in this case, blood cells,and not, for example, cells of the nervous systemor the skeletal system. so, our hematopoietic stem cells are always busy churningout new blood cells, red blood cells to carry oxygen for us, and white blood cells to keep our immune system nice and strong. and for a more clinical example,

with blood diseases like leukemia, certain blood cellswill grow uncontrollably within a patient's bone marrow, and it actually crowds out their healthy stem cells, here, from being able to produce enough blood cells. so, as part of treatment,once the leukemia cells are cleared from the bone marrowwith, usually, chemotherapy or radiation, doctors can actually put

more hematopoietic stem cellsback into the bone marrow that then go on to produce normal amounts of blood for the person again. so, this is probably the most common use of stem cells in medicine as of now. and you can actually findthese multipotent stem cells in most tissues and organs. so, for example, we havemultipotent neural stem cells that slowly give rise to neurons

and their supporting cells when necessary. and we have multipotentmesenchymal stem cells in a few different places in the body that give rise to bonecells and cartilage cells, and adipose cells. so, you might be wonderingafter seeing our epithelial and our hematopoietic stem cells dividing, why aren't these cells beingused up as they divide? and that's a really good question.

so, stem cells havetwo mechanisms in place to make sure that theirnumbers are maintained. so, their first trick isthat when they divide, they undergo what's calledobligate asymmetric replication where the stem cell dividesinto one so called mother cell identical to the original stem cell, and one daughter cellthat's differentiated. so, then, the daughtercell can go on to become more specialized while the mother cell

replaces the stem cellthat divided, initially. the other mechanism is calledstochastic differentiation. so, if one stem cellhappens to differentiate into two daughter cells insteadof a mother and a daughter, another stem cell will notice this and makes up for the lossof the original stem cell by undergoing mitosis andproducing two stem cells identical to the original. so, these two mechanisms make sure

their numbers remain nice and strong. so, we've looked at embryonic stem cells and we've looked at somatic stem cells. there's actually one more type called induced pluripotent stemcells, or ips cells. it turns out that youcan actually introduce a few specific genes intoalready specialized somatic cells like muscle cells, andthey'll sort of forget what type of cell they are,and they'll revert back,

they'll be reprogrammedinto a pluripotent stem cell just like an embryonic stem cell. and this is a huge discovery. i mean, the technique isstill being perfected, but, there's a lot ofmedicinal implications, here. for example, ips cellsare basically the core of regenerative medicine,which is a pretty new field of medicine where the goalis to repair damaged tissues in a given person by using stem cells

from their own body. so, with ips cells, each patient can have their own pluripotent stem cell line to theoretically replaceany damaged organs with new ones made out of their own cells. so, not only would apatient get the new organ they might need, but, there also won't be any immune rejection complications since the cells are their own.

so, there's still a ways to go here before this type of medicineis sort of mainstream, but, already, ips cells have helped to create the precursorsto a few different human organs in labs, suchas the heart and the liver. now, before we finish up here, i just wanna answer two questions that might have come up for you. so, one, what triggers ourstem cells to differentiate?

well, it turns out thatin normal situations, right, when the stemcell's just hangin' out, not doin' too much, it actually expresses a few different genes that helps to keep it undifferentiated. so, there are a few proteinsfloating around in the cell that prevents other genesfrom being activated and triggering differentiation. but, when put in certain environments,

this regulation can be overridden, and then, they can go on and differentiate into a more specialized cell. the type of which depends on what specific little chemical signals are hanging around in the stem cell's environment. so, for example, in the bone marrow, there are certain proteinsthat hang around stem cells and induce some to differentiate

into the specific blood cell types. and finally, what's all thisstuff you might have heard, maybe in the news, about cord blood? well, from cord blood,which is blood taken from the placenta and the umbilical cord after the birth of ababy, you can get lots of multipotent stem cells, and sometimes, some other stem cells that have been shown to be pluripotent.

so, this cord blood usedto just be discarded after a baby's birth, but now, there's a lot of interest in keeping it because now we know itcontains all these stem cells.

how to get stem cells

how to get stem cells

i want to tell you one story. and the storycame from the early 1950s. a woman named wanda ruth lunsford, she was a scientist in newyork city and she published one paper, which turned out to be her only paper in scienceand she was actually pushed out of science. what she did was she took an old rat and ayoung rat, she put them to sleep and she tied their skin together. so after about a dayor so their blood supplies joined. well, several weeks later she looked and in that old ratthere were new neurons growing in the brain, the heart beat stronger and the muscles werebigger. the gray hair turned brown again. she claimed she reversed aging. people callher dracula, frankenstein, all kinds of crazy names.

well, earlier this year three separate laboratoriesat harvard, stanford, university of california san francisco repeated the experiment andit worked. and what they showed is at age 25, in you and i, our stem cells go to sleepand get turned off. and proteins, from young mice in this case or young humans, can turnthem back on again. and when these stem cells get turned back on new neurons can be grown,repair happens much quicker in tissue. we all see that. our child breaks his leg heor she is back walking again in a couple weeks. you don't even know what happened. your grandmotherbreaks her leg and it hits her quality of life the rest of her life. so there are clinicaltrials now using proteins that were found in young individual to try to stimulate bonerepair in the elderly who have fractures.

and so just like a diabetic requires a shotof insulin so that they can manage their sugar, going forward if you break your leg in theelderly we may just give you a shot of these proteins to turn back on your stem cells soyou can repair quicker. we're trying it in cancer because cancer inkids is about 90 percent curable. once you turn 25 that same cancer turns incurable.so maybe if i can convince the body it's younger i can have, or we as a science community canhave, a bigger impact on cancer. so i leave you with that bit of hope that aging is somethingthat may be able to be reversed, and not so that we can live till 150 but so that we canall live until our ninth or tenth decade without there being a decrease in quality in thoselast decades, because that would be the goal,

quality years till the end.

how do you get stem cells

how do you get stem cells

embryonic stem cells are a huge next stepfor medicine, but they’re mired in controversy. so what if you could have all the benefitsof regenerative medicine, without the thorny moral dilemma? hello science lovers, julian here for dnews.there’s been a huge breakthrough in medicine this week; induced pluripotent stem cellswere used in a tissue transplant for the first time ever. we did it! yeah!! oh am i goingto need to explain that? ok. first, let’s get everybody up to speed onstem cells. this is more important to you than you realize because you were at somepoint nothing more than 50 to 150 of them. you probably don’t remember, it was only4 days after you were conceived.

what makes embryonic stem cells amazing isthey are pluripotent, meaning they can become almost any type of cell. this means they canbe used to replace damaged tissue and may one day be an alternative to organ transplants.this is huge. in the united states an average of 79 people receive an organ transplant everyday, but another 18 people die waiting for a transplant that will never come. the 79 who do get a donor will have to takemedication to prevent transplant rejection for the rest of their lives, but even thenthe risk remains. that problem doesn’t exist with embryonic stem cells. so we can savethousands of people a year and improve the quality of life and lifespan of tens of thousandsmore. what’s the problem here?

well the only way to get pluripotent cellsis from embryos. which are pre-people. or current people, depending on where you standon the issue. obviously, there’s a heated controversy there and i’m sure the commentswill reflect that (be nice, guys). umbilical cord blood has multipotent stem cells, butthey’re more limited. and we all have adult stem cells but those are even less versatile.so there are no alternatives. until now. shinya yamanaka of kyoto university discovereda method to create pluripotent stem cells from adult cells. it’s like diet stem cells:all of the flavor with none of the calories. though “flavor” in this case means life-changingbenefits and “calories” means severe moral dilemma of using undeveloped humans in medicine.and for his breakthrough, yamanaka shared

the nobel prize for physiology in 2012. and now, here we are, september 2014, whereon friday, at 2:20 local time, japanese doctors stopped the macular degeneration of a 70 year-oldwoman by transplanting a sheet of retinal pigment epithelium cells derived from inducedpluripotent stem cells made from reprogrammed cells of the patient’s own skin! we didit! probably! now we wait and see if the procedure checks the macular degeneration without becomingcancerous or rejected. by the way the sheet of tissue used was just3 by 1.3mm. that’s about that big. and what a huge step that is. if you’d like to learn more about how youreye works and why the macula is important

to vision, check out this video. as a bonus,you can stare deep into trace’s dreamy, dreamy eyes. can you think of any creative potential usesfor induced pluripotent stem cells *cough* wolverine *cough*? let us know in the comments.hopefully it stems productive discussion. remember to subscribe for the latest in science,and i’ll see you next time on dnews.

how do we get stem cells

how do we get stem cells

this video will show you how to passage pscswith edta in essential 8™ medium on vitronectin coated plates. the following protocol uses a 6-well plate.if you’re using another type of cell culture vessel, please refer to table 2 on the writtenprotocol for volumes there are three major differences that you’llobserve with cells cultured in essential 8™ medium on vitronectin compared to other feeder-freesystems such as mtesr and stempro hesc sfm: • cells are typically passaged ~24 hourssooner than they would be with other feeder-free media.• passaging should take place when cells are at ~85% confluency. if cells are passagedwhen they are more than 85% confluent, the

health of the cells and final cell yield maybe compromised. • cells must be passaged in edta. collagenaseand dispase are not recommended. cells will reach optimal confluency typicallyevery four to five days. you should also split cultures or passagecells when psc colonies become too dense or too large or show increased differentiation; the split ratio can vary, although it’sgenerally between 1:2 and 1:4 for early passages and between 1:3 and 1:12 for established cultures.occasionally, cells will grow at a different rate and the split ratio will need to be adjusted. a good rule is to observe the last split ratioand adjust the ratio according to the appearance

of the psc colonies. if the cells look healthy,and the colonies have enough space, split your cultures using the same ratio. if thecolonies are overly dense and crowding, increase the ratio; if they are sparse, decrease theratio. newly derived psc lines may contain a fairamount of differentiation through passage 4. it’s not necessary to remove differentiatedmaterial prior to passaging. by propagating/splitting the cells, the overall health of the cultureshould improve throughout the early passages. prepare 0.5 mm edta by combining 50 âµl ofultrapureâ„¢ 0.5 m edta, ph 8.0 with 50 ml of dpbs without calcium and magnesium. filter,sterilize the solution. and store at room temperature.

pre-warm complete essential 8â„¢ medium andvtn-n-coated culture vessels to room temperature. aspirate the spent medium from the vesselcontaining pscs and rinse the vessel twice with dpbs without calcium and magnesium. add 0.5 mm edta in dpbs to the vessel containingpscs. swirl the vessel to coat the entire cell surface. incubate the vessel at room temperature for5 to 8 minutes or at 37 degrees celsius for 4 to 5 minutes. when the cells start to separateand round up, and the colonies appear to have holes in them when viewed under a microscope,they are ready to be removed from the vessel. note: in larger vessels or with certain celllines, this may take longer than 5 minutes.

aspirate the edta solution, and add pre-warmedessential 8â„¢ medium to the vessel. remove the cells from the well(s) by gentlysquirting medium and pipetting the colonies up. avoid creating bubbles. try to work with no more than 1 to 3 wellsat a time, and work quickly to remove cells after adding essential 8â„¢ medium to thewell(s), which quickly neutralizes the initial effect of the edta. some lines re-adhere veryrapidly after medium addition, and must be removed 1 well at a time. others are slowerto re-attach, and may be removed 3 wells at a time. collect cells in a 15ml conical tube. theremay be obvious patches of cells that were

not dislodged and left behind. don’t scrapethe cells from the dish in an attempt to recover them. add an appropriate volume of pre-warmed essential8™ medium to each well of a vitronectin coated 6-well plate so that each well contains2 ml of medium after the cell suspension has been added. move the vessel in several quick figure eightmotions to disperse the cells across the surface of the vessels. place the vessel gently intothe 37 degrees celsius, 5% co2 incubator and incubate the cells overnight. feed the psc cells with essential 8™ mediumbeginning the second day after splitting and

replace the spent medium daily. it is normal to see cell debris and smallcolonies after passage.

how do stem cells work

how do stem cells work

can you imagine a world where one day if youneed a new heart you could just order one made just for you? sound like science fiction?well we’re not so far off. hey guys, julia here for dnews dudes, so something pretty cool just happenedin the wonderful world of science. researchers grew beating hearts from human stem cells.okay fine hyperbole, it’s not the whole heart just a few beating cells. but it’sso cool. in a study published in the journal nature,the researchers used human skin cells, turned them into pluripotent cells and used physicaland chemical signals to coax the cells into forming little cardiac microchambers. whichcould be important for studying how the heart

grows in an embryo or how drugs might affecta fetus’s heart. or… looking way into the future, for growing hearts in a dish.it could be a great way to replace organs. no more waiting for a donor and since it wouldbe perfect match to your body, no more terrible drugs to prevent rejection.so far smaller organs like tracheas and bladders have been grown in a lab using a person’sown stem cells, but a heart is a little more complicated. so let’s take a little lookinto how we got here. first off, what are stem cells? stem cellsare pluripotent, meaning they are undifferentiated cells that can develop into any kind of cell.skin, heart, liver etc. so alright, but what’s the big deal? why do researchers love to studystem cells? even from the earliest inklings

of stem cells, there have been big dreams.researchers have hoped that one day they could be able to grow entire new organs from stemcells that would be a perfect match for the recipient. we’ve come a long way from the early daysof stem cell research. human stem cells were first isolated in 1998 by two independentresearch teams led by james a. thomson of the university of wisconsin and another byjohn d. gearhart of johns hopkins university school of medicine. these early stem celllines were derived from early embryos, which are destroyed in the process and thus stirreda little controversy. okay a lot of controversy. because of the debate that raged in the ussurrounding embryonic stem cell research,

scientists looked to find stem cells in otheradult tissues. so a few years later in 2001 adult stem cells were found in fat tissue.now adult stem cells can be found from almost any tissue. but they are tricky, they takea while to coax into growing in a dish. so they’re not ideal. but in 2007, in a paper published in the journalnature biotechnology, dr. anthony alata discovered that amniotic fluid also contains stem cells.which of course added more fuel to the debate. and the same year, two independent teams ofresearchers pioneered a process to turn adult somatic cells into pluripotent stem cells,naturally called induced pluripotent stem cells. the process involves introducing 4different genes into the cells using a virus

as a carrier. the team from japan led shinya yamanaka, publishedtheir work in the journal cell and the team from by james thomson at university of wisconsin–madisonpublished their work in the journal nature. and it was such a huge deal that, yamanakaactually won the 2012 nobel prize for discovering ips cells. which of course this discovery held a lotof promise, it would sidestep some of the controversy with embryonic stem cells. butthere are more than a few issues with their technique, like low efficiency, it’s difficultto do and when done, only a few cells are reprogrammed. plus there’s weird problemswith rejection and also a problem with tumors

developing. but problems aside, tons of studies have beenand are being done with this technology. with lofty goals, like attempting to cure blindnessand diabetes. the federation of american societies for experimental biology says that ips cellswill also “allow scientists to study complex human diseases in petri dishes, a step towardanalyzing the conditions and developing therapies.” some researchers like dr. alata don’t carewhere the cells come from, just that they work well. no matter where stem cells comefrom, it’s clear that we’re on the road to organs grown in a dish. well i certainlyhope so. but it’s also clear that more research is needed.

and really, lab grown organs can’t comesoon enough! if you wanna know the challenges of living with an organ transplant & why theyfail, check out this recent video i did:

how are stem cells used

how are stem cells used

[ music ] >> hello. i'm dr.elias zambidis. i'm a pediatric bonemarrow transplant physician at johns hopkins. as a practicing physician andscientist, i care for children with leukemia andother blood disorders. my laboratory studiesof very special class of human stem cells calledhuman pluripotent stem cells that can make anypart of the body.

i'm interested inexpanding my practice as a transplant physician touse human pluripotent stem cells for treating diseases such ascancer, autoimmune disease, and vascular disorders. recently, my lab generatedclinically useful human pluripotent stem cells fortreating vascular disorders.

how are stem cells obtained

how are stem cells obtained

embryonic stem cells are a huge next stepfor medicine, but they’re mired in controversy. so what if you could have all the benefitsof regenerative medicine, without the thorny moral dilemma? hello science lovers, julian here for dnews.there’s been a huge breakthrough in medicine this week; induced pluripotent stem cellswere used in a tissue transplant for the first time ever. we did it! yeah!! oh am i goingto need to explain that? ok. first, let’s get everybody up to speed onstem cells. this is more important to you than you realize because you were at somepoint nothing more than 50 to 150 of them. you probably don’t remember, it was only4 days after you were conceived.

what makes embryonic stem cells amazing isthey are pluripotent, meaning they can become almost any type of cell. this means they canbe used to replace damaged tissue and may one day be an alternative to organ transplants.this is huge. in the united states an average of 79 people receive an organ transplant everyday, but another 18 people die waiting for a transplant that will never come. the 79 who do get a donor will have to takemedication to prevent transplant rejection for the rest of their lives, but even thenthe risk remains. that problem doesn’t exist with embryonic stem cells. so we can savethousands of people a year and improve the quality of life and lifespan of tens of thousandsmore. what’s the problem here?

well the only way to get pluripotent cellsis from embryos. which are pre-people. or current people, depending on where you standon the issue. obviously, there’s a heated controversy there and i’m sure the commentswill reflect that (be nice, guys). umbilical cord blood has multipotent stem cells, butthey’re more limited. and we all have adult stem cells but those are even less versatile.so there are no alternatives. until now. shinya yamanaka of kyoto university discovereda method to create pluripotent stem cells from adult cells. it’s like diet stem cells:all of the flavor with none of the calories. though “flavor” in this case means life-changingbenefits and “calories” means severe moral dilemma of using undeveloped humans in medicine.and for his breakthrough, yamanaka shared

the nobel prize for physiology in 2012. and now, here we are, september 2014, whereon friday, at 2:20 local time, japanese doctors stopped the macular degeneration of a 70 year-oldwoman by transplanting a sheet of retinal pigment epithelium cells derived from inducedpluripotent stem cells made from reprogrammed cells of the patient’s own skin! we didit! probably! now we wait and see if the procedure checks the macular degeneration without becomingcancerous or rejected. by the way the sheet of tissue used was just3 by 1.3mm. that’s about that big. and what a huge step that is. if you’d like to learn more about how youreye works and why the macula is important

to vision, check out this video. as a bonus,you can stare deep into trace’s dreamy, dreamy eyes. can you think of any creative potential usesfor induced pluripotent stem cells *cough* wolverine *cough*? let us know in the comments.hopefully it stems productive discussion. remember to subscribe for the latest in science,and i’ll see you next time on dnews.

history of stem cells

history of stem cells

- [voiceover] so, let megive you an analogy, here. when you were still anadorable little baby, you were just bursting with potential. you could decide to be a pilot, or a doctor, or a journalist. you had the potential to specialize into all sorts of different careers, and as you got a bit older,you got more and more committed down a certain pathway,

and the decisions that you made moved you further and furtheralong this pathway, right? well, it turns out that stemcells operate in a similar way, going from unspecializedto more specialized as they get older. so, let me show you what i mean by that over the course of this video. and let's actually startback at the zygote, here, the cell that resultswhen sperm and egg fuse

because that's really where our stem cell story kinda begins. so, the zygote starts to divide, right, by mitosis until it reachesthe blastocyst stage, this hollow ball of cellshere is called a blastocyst. and here, things start to geta little bit more interesting. so, in a blastocyst, there'sthis little grouping of cells down in here, referred toas the inner cell mass. and this is a really speciallittle bunch of cells

that go on to become the embryo. so, these are called stem cells. and what they can do as stem cells is they can specialize intoseveral other cell types. so, we actually call thempluripotent stem cells. pluri meaning several and potent referring to these stem cells' ability to actually do this differentiation. so, during development,these inner cell mass

pluripotent stem cells can differentiate into any of the more than200 different cell types in the adult human body whengiven the proper stimulation. so, it's kind of incredible to think that every single cell in your body can trace its ancestry back to this little group of stem cells, here. and actually, if you ever hear anyone talking about embryonic stem cells,

these are the ones they're referring to, these icm stem cells. so, is this the only placewe can find stem cells, here in the developmental structures? we used to think so, but, it turns out that in mammals, there aretwo main types of stem cells. embryonic stem cells that we just saw and somatic stem cells whichare found in every person. so, the embryonic stem cellsare used to build our bodies,

to go from one cell totrillions of specialized cells, and the somatic stem cells are used as sort of a repair system for the body, replenishing tissuesthat need to be replaced. and they can't repair everything, but, there's a lot of every day repairs that can happen because of our stem cells. so, in skin, for example... this outside layer is the partof our skin that we can see

and that we can touch, right? and it's made of these waterproof, pretty rugged epithelialor skin cells and interestingly, althoughthey are pretty rugged, you're constantlyshedding these skin cells. they actually just sort offall off or get rubbed off during every day activities like when you're putting your clothes on. and then, the ones from underneath them

just sort of move up and take their place. so, you shed them and you lose almost 40,000 of them per hour. so, if we wanna have anyhope of keeping our skin, we kinda need a way toreplace these cells, and that's where stem cells that live in our skin come in. actually, our skin cells are shed and replaced so often,that it only takes a month

for us to have a completely new skin. like, literally onemonth, entirely new skin. it's outrageous. anyway, deep within our skin, there's this layer of stem cells called epidermal stem cells, and their job is to becontinually dividing. so, you can see themdividing, here, dividing, dividing, dividing, and makingnew skin cells that go on

to migrate upward as themultiple layers of our skin. and their goal is to eventually replace these ones up here on the outside that get damaged or worn out and fall off. so, it's this kind of activity here which show off our stem cells' role as our regenerative cells. now, lemme just highlighta few differences between our mature skin cells over here

and our stem cells down here. they are very different. mature cells are notthe same as stem cells, and this principle goesfor really any mature cell versus any stem cell. so, the mature cell isalready specialized, it already has a really specific function. for example, our outer layerof epithelial cells, here, they have a protective function

against the outside environment. and, you know, just thinkingof other adult cell types, right, like muscle cellshave a contractile function, and neurons have amessage sending function, and bones have a rigidstructural function. so, all these adult cells are already nice and specialized, they'vegrown up and decided what they wanna do for a living, whereas, stem cells arenot like that at all.

stem cells are unspecialized. but, they still have areally important job, which is to give rise to ourmore specialized cell types, like these cells here, okay? and, actually, in order tobe considered a stem cell, and this goes for theembryonic stem cells we met previously and the somaticstem cells we're meeting now, to be a stem cell, you'd need to possess two main properties.

the ability to self renew,meaning you can divide and divide, and divide, but, at least one of your resultingcells remains a stem cell, it remains undifferentiated, and you'd need to have a high capacity to differentiate intomore specialized cells when the time comes. so, remember, this is also referred to as having some degree of potency.

and there's actually a few different types of stem cells, and someof them can turn into more types of cells than others. some are more potent than others. so, this epithelial stem cell we saw here is actually one of the lesspotent types of stem cell. in other words, thesestem cells can only divide and specialize into more epithelial cells. so, they're our source ofepithelial cells, sure,

but, only epithelial cellsand not any other cell type. so, we call them unipotent,referring to their ability to only create one type of cell. but, lemme show you another example here of a multipotent stem cell. let's look at this guy'sfemur, his thigh bone, which is where our blood cells are made inside bone marrow in our bones. so, you might know thatour red blood cells

have a life span of about four months. so, that means that we needto be constantly replacing our red blood cells orwe'll run out, right? well, in our bone marrow,we have what are called hematopoietic stem cells, which are our blood making stem cells. and these are pretty special, they're multipotent stem cells, which means they can giverise to many types of cells,

but, only ones within a specific family. in this case, blood cells,and not, for example, cells of the nervous systemor the skeletal system. so, our hematopoietic stem cells are always busy churningout new blood cells, red blood cells to carry oxygen for us, and white blood cells to keep our immune system nice and strong. and for a more clinical example,

with blood diseases like leukemia, certain blood cellswill grow uncontrollably within a patient's bone marrow, and it actually crowds out their healthy stem cells, here, from being able to produce enough blood cells. so, as part of treatment,once the leukemia cells are cleared from the bone marrowwith, usually, chemotherapy or radiation, doctors can actually put

more hematopoietic stem cellsback into the bone marrow that then go on to produce normal amounts of blood for the person again. so, this is probably the most common use of stem cells in medicine as of now. and you can actually findthese multipotent stem cells in most tissues and organs. so, for example, we havemultipotent neural stem cells that slowly give rise to neurons

and their supporting cells when necessary. and we have multipotentmesenchymal stem cells in a few different places in the body that give rise to bonecells and cartilage cells, and adipose cells. so, you might be wonderingafter seeing our epithelial and our hematopoietic stem cells dividing, why aren't these cells beingused up as they divide? and that's a really good question.

so, stem cells havetwo mechanisms in place to make sure that theirnumbers are maintained. so, their first trick isthat when they divide, they undergo what's calledobligate asymmetric replication where the stem cell dividesinto one so called mother cell identical to the original stem cell, and one daughter cellthat's differentiated. so, then, the daughtercell can go on to become more specialized while the mother cell

replaces the stem cellthat divided, initially. the other mechanism is calledstochastic differentiation. so, if one stem cellhappens to differentiate into two daughter cells insteadof a mother and a daughter, another stem cell will notice this and makes up for the lossof the original stem cell by undergoing mitosis andproducing two stem cells identical to the original. so, these two mechanisms make sure

their numbers remain nice and strong. so, we've looked at embryonic stem cells and we've looked at somatic stem cells. there's actually one more type called induced pluripotent stemcells, or ips cells. it turns out that youcan actually introduce a few specific genes intoalready specialized somatic cells like muscle cells, andthey'll sort of forget what type of cell they are,and they'll revert back,

they'll be reprogrammedinto a pluripotent stem cell just like an embryonic stem cell. and this is a huge discovery. i mean, the technique isstill being perfected, but, there's a lot ofmedicinal implications, here. for example, ips cellsare basically the core of regenerative medicine,which is a pretty new field of medicine where the goalis to repair damaged tissues in a given person by using stem cells

from their own body. so, with ips cells, each patient can have their own pluripotent stem cell line to theoretically replaceany damaged organs with new ones made out of their own cells. so, not only would apatient get the new organ they might need, but, there also won't be any immune rejection complications since the cells are their own.

so, there's still a ways to go here before this type of medicineis sort of mainstream, but, already, ips cells have helped to create the precursorsto a few different human organs in labs, suchas the heart and the liver. now, before we finish up here, i just wanna answer two questions that might have come up for you. so, one, what triggers ourstem cells to differentiate?

well, it turns out thatin normal situations, right, when the stemcell's just hangin' out, not doin' too much, it actually expresses a few different genes that helps to keep it undifferentiated. so, there are a few proteinsfloating around in the cell that prevents other genesfrom being activated and triggering differentiation. but, when put in certain environments,

this regulation can be overridden, and then, they can go on and differentiate into a more specialized cell. the type of which depends on what specific little chemical signals are hanging around in the stem cell's environment. so, for example, in the bone marrow, there are certain proteinsthat hang around stem cells and induce some to differentiate

into the specific blood cell types. and finally, what's all thisstuff you might have heard, maybe in the news, about cord blood? well, from cord blood,which is blood taken from the placenta and the umbilical cord after the birth of ababy, you can get lots of multipotent stem cells, and sometimes, some other stem cells that have been shown to be pluripotent.

so, this cord blood usedto just be discarded after a baby's birth, but now, there's a lot of interest in keeping it because now we know itcontains all these stem cells.

history of stem cell research

history of stem cell research

it's just beautiful, isn't it? it's just mesmerizing.it's double hel-exciting! you really can tell, just by looking at it,how important and amazing it is. it's pretty much the most complicated moleculethat exists, and potentially the most important one. it's so complex that we didn't even knowfor sure what it looked like until about 60 years ago. so multifariously awesome that if you tookall of it from just one of our cells and untangled it, it would be taller than me. now consider that there are probably 50 trillioncells in my body right now. laid end to end, the dna in those cells wouldstretch to the sun.

not once... but 600 times! mind blown yet? hey, you wanna make one? (oh dear god) of course you know i'm talking about deoxyribonucleicacid, known to its friends as dna. dna is what stores our genetic instructions-- the information that programs all of our cell's activities. it's a 6-billion letter code that providesthe assembly instructions for everything that you are.

and it does the same thing for pretty muchevery other living thing. i'm going to go out on a limb and assumeyou're human. in which case every body cell, or somaticcell, in you right now, has 46 chromosomes each containing one big dna molecule. these chromosomes are packed together tightlywith proteins in the nucleus of the cell. dna is a nucleic acid. and so is its cousin, which we'll also betalking about, ribonucleic acid, or rna. now if you can make your mind do this, rememberall the way back to episode 3, where we talked about all the important biological molecules:

carbohydrates, lipids and proteins. that ringa bell? well nucleic acids are the fourth major groupof biological molecules, and for my money they have the most complicated job of all. structurally they're polymers, which meansthat each one is made up of many small, repeating molecular units. in dna, these small units are called nucleotides.link them together and you have yourself a polynucleotide. now before we actually put these tiny partstogether to build a dna molecule like some microscopic piece ofikea furniture, let's

first take a look at what makes up each nucleotide. we're gonna need three things: 1. a five-carbon sugar molecule 2. a phosphate group 3. one of four nitrogen bases dna gets the first part its name from ourfirst ingredient, the sugar molecule, which is called deoxyribose. but all the really significant stuff, thegenetic coding that makes you you, is found among the four nitrogenous bases:

adenine (a), thymine (t), cytosine (c) andguanine (g). it's important to note that in living organisms,dna doesn't exist as a single polynucleotide molecule, but rathera pair of molecules that are held tightly together. they're like an intertwined, microscopic,double spiral staircase. basically, just a ladder, but twisted. thefamous double helix. and like any good structure, we have to havea main support. in dna, the sugars and phosphates bond togetherto form twin backbones. these sugar-phosphate bonds run down eachside of the helix but, chemically, in opposite directions.

in other words, if you look at each of thesugar-phosphate backbones, you'll see that one appears upside-down in relation to theother. one strand begins at the top with the firstphosphate connected to the sugar molecule's 5th carbon and then ending where the nextphosphate would go, with a free end at the sugar's 3rd carbon. this creates a pattern called 5' (5 prime)and 3' (3 prime). i've always thought of the deoxyribose withan arrow, with the oxygen as the point. it always 'points' from from 3' to 5'.

now on the other strand, it's exactly theopposite. it begins up top with a free end at the sugar's3rd carbon and the phosphates connect to the sugars' fifth carbons all the way down. and it ends at the bottom with a phosphate. and you've probably figured this out already,but this is called the 3' to 5' direction. now it is time to make ourselves one of thesefamous double helices. these two long chains are linked by the nitrogenousbases via relatively weak hydrogen bonds. but they can't be just any pair of nitrogenousbases. thankfully, when it comes to figuring outwhat part goes where, all you have to do is

remember is that if one nucleotide has anadenine base (a), only thymine (t) can be its counterpart (a-t). likewise, guanine (g) can only bond with cytosine[c] (g-c). these bonded nitrogenous bases are calledbase pairs. the g-c pairing has three hydrogen bonds,making it slightly stronger than the a-t base-pair, which only has two bonds. it's the order of these four nucleobasesor the base sequence that allows your dna to create you. so, aggtccatg means something completely differentas a base sequence than, say, ttcagtcg.

human chromosome 1, the largest of all ourchromosomes, contains a single molecule of dna with 247 million base pairs. if you printed all of the letters of chromosome1 into a book, it would be about 200,000 pages and each of your somatic cells has 46 dnamolecules tightly packed into its nucleus -- that's one for each of your chromosomes. put all 46 molecules together and we'retalking about roughly 6 billion base pairs .... in every cell! this is the longest book i've ever read. it's about 1,000 pages long.

if we were to fill it with our dna sequence,we'd need about 10,000 of them to fit our entire genome. pop quiz!!! let's test your skills using a very shortstrand of dna. i'll give you one base sequence -- yougive me the base sequence that appears on the other strand. okay, here goes: 5' -- aggtccg -- 3' and... time's up.

the answer is: 3' -- tccaggc -- 5' see how that works? it's not super complicated. since each nitrogenous base only has one counterpart,you can use one base sequence to predict what its matching sequence is going to look like. so could i make the same base sequence witha strand of that "other" nucleic acid, rna? no, you could not. rna is certainly similar to its cousin dna-- it has a sugar-phosphate backbone with

nucleotide bases attached to it. but there are three major differences: 1. rna is a single-stranded molecule -- nodouble helix here. 2. the sugar in rna is ribose, which has onemore oxygen atom than deoxyribose, hence the whole starting with an r instead of a d thing. 3. also, rna does not contain thymine. itsfourth nucleotide is the base uracil, so it bonds with adenine instead. rna is super important in the production ofour proteins, and you'll see later that it has a crucial role in the replication ofdna.

but first... biolo-graphies! yes, plural this week! because when you start talking about somethingas multitudinously awesome and elegant as dna, you have to wonder: who figured all of this out? and how big was their brain? well unsurprisingly, it actually took a lotof different brains, in a lot of different countries

and nearly a hundred years of thinking todo it. the names you usually hear when someone askswho discovered dna are james watson and francis crick. but that's bunk. they did not discover dna. nor did they discover that dna contained geneticinformation. dna itself was discovered in 1869 by a swissbiologist named friedrich miescher. his deal was studying white blood cells. and he got those white blood cells in themost horrible way you could possibly imagine, from collecting used bandages from a nearbyhospital.

it's for science he did it! he bathed the cells in warm alcohol to removethe lipids, then he set enzymes loose on them to digestthe proteins. what was left, after all that, was snottygray stuff that he knew must be some new kind of biological substance. he called it nuclein, but was later to becomeknown as nucleic acid. but miescher didn't know what its role wasor what it looked like. one of those scientists who helped figurethat out was rosalind franklin, a young biophysicist in london nearly a hundred years later.

using a technique called x-ray diffraction,franklin may have been the first to confirm the helical structure of dna. she also figured out that the sugar-phosphatebackbone existed on the outside of its structure. so why is rosalind franklin not exactly ahousehold name? two reasons: 1. unlike watson & crick, franklin was happyto share data with her rivals. it was franklin who informed watson & crick that an earliertheory of a triple-helix structure was not possible,and in doing so she indicated that dna may indeed be a double helix. later, her images confirming the helical structureof dna were shown to watson without her knowledge.

her work was eventually published in nature,but not until after two papers by watson and crick had already appeared in which the duoonly hinted at her contribution. 2. even worse than that, the nobel prize committeecouldn't even consider her for the prize that they awarded in 1962 because of how deadshe was. the really tragic thing is that it's totallypossible that her scientific work may have led to her early death of ovarian cancer atthe age of 37. at the time, the x-ray diffraction technologythat she was using to photograph dna required dangerous amounts of radiation exposure, andfranklin rarely took precautions to protect herself. nobel prizes cannot be awarded posthumously.many believe she would have shared watson

and crick's medal if she had been aliveto receive it. now that we know the basics of dna's structure,we need to understand how it copies itself, because cells are constantly dividing, andthat requires a complete copy of all of that dna information. it turns out that our cells are extremelygood at this -- our cells can create the equivalent 10,000 copies of this book in justa few hours. that, my friends, is called replication. every cell in your body has a copy of thesame dna. it started from an original copy and it will copy itself trillions of timesover the course of a lifetime, each time using

half of the original dna strand as a templateto build a new molecule. so, how is a teenage boy like the enzyme helicase? they both want to unzip your genes. (hank why) helicase is marvelous, unwinding the doublehelix at breakneck speeds, slicing open those loose hydrogen bonds between the base pairs. the point where the splitting starts is knownas the replication fork, has a top strand, called the leading strand, or the good guystrand as i call it and another bottom strand called the laggingstrand, which i like to call the scumbag strand, because it is a pain in the butt to deal with.

these unwound sections can now be used astemplates to create two complementary dna strands. but remember the two strands go in oppositedirections, in terms of their chemical structure, which means making a new dna strand for theleading strand is going to be much easier for the lagging strand. for the leading, good guy, strand an enzymecalled dna polymerase just adds matching nucleotides onto the main stem all the way down the molecule. but before it can do that it needs a sectionof nucleotides that fill in the section that's just been unzipped. starting at the very beginning of the dnamolecule, dna polymerase needs a bit of a

primer, just a little thing for it to hookon to so that it can start building the new dna chain. and for that little primer, we can thank theenzyme rna primase. the leading strand only needs this rna primeronce at the very beginning. then dna polymerase is all, "i got this" and just follows the unzipping, adding newnucleotides to the new chain continuously, all the way down the molecule. copying the lagging, or scumbag strand, is, well, he's a freaking scumbag.

this is because dna polymerase can only copystrands in the 5' -- 3' direction, and the lagging strand is 3' -- 5', so dna polymerase can only add new nucleotidesto the free, 3' end of a primer. so maybe the real scumbag here is the dnapolymerase. since the lagging strand runs in the oppositedirection, it has to be copied as a series of segments. here that awesome little enzyme rna primasedoes its thing again, laying down an occasional short little rna primer that gives the dnapolymerase a starting point to then work backwards along the strand.

this is done in a ton of individual segments,each 1,000 to 2,000 base pairs long and each starting with an rna primer, called okazakifragments after the couple of married scientists who discovered this step of the process inthe 1960s. and thank goodness they were married so wecan just call them okazaki fragments instead of okazaki-someone's-someone fragments. these allow the strands to be synthesizedin short bursts. then another kind of dna polymerase has togo back over and replace all those rna primers and then all of the little fragments get joinedup by a final enzyme called dna ligase. and that is why i saythe lagging strand is such a scumbag!

dna replication gets it wrong about one inevery 10 billion nucleotides. but don't think your body doesn't havean app for that! it turns out dna polymerases can also proofread,in a sense, removing nucleotides from the end of a strandwhen they discover a mismatched base. because the last thing we want is an a whenit would have been a g! considering how tightly packed dna is intoeach one of our cells, it's honestly amazing that more mistakes don't happen. remember, we're talking about millions ofmiles worth of this stuff inside us. and this, my friends, is why scientists arenot exaggerating when they call dna the most

celebrated molecule of all time. so, you might as well look this episode overa couple of times and appreciate it for yourself. and in the mean time, gear up for next week,when we're going to talk about how those six feet of kick-ass actually makes you, you. thank you to all the people here at crashcourse who helped make this episode awesome. you can click on any of these things to goback to that section of the video. if you have any questions, please, of course,ask them in the comments or on facebook or twitter.

hematopoietic stem cells

hematopoietic stem cells

placidway is the leading medical tourism companythat helps you compare and customize the most affordable treatments worldwide. placidwayplacidway, is a leader in medical travel. and helps people find the best package fortheir treatments. like with connor,he needed a bone marrow transplantbut he hadn't got enough money for the treatment. when he contacted placidway he learned thathe can have affordable packages travelling abroad. so he chose bone marrow stem cells in mumbai,india.. by reelabs.

the stem cell samples in reelabs are collected,processed and stored as per international standards that ensure optimum yield of stemcells. reelabs is a highly sophisticated, state-of-the-artstem cell facility that employs a quality management system based on continuous improvement,to ensure that all aspects of its services are consistently carried out and meets internationalcellular therapy standards. if you want to know more, contact us. subscribe to our you tube channel and getinstant access to all of our latest medical care videos. enjoy your free pass to quality global healthcare!

heart stem cells

heart stem cells

studies on human embryonic stem cells arehighly controversial, and the current law says that embryos must be destroyed after14-days. but why 14-days? what’s so significant about the two week limit, and should we evenkeep using it? hi there my science buddies. julian here fordnews. human embryonic stem cells are one of the most legally and morally contentiousareas of study. on the one hand, stem cells, both adult and embryonic, are valuable forresearching a huge range of illnesses and diseases, from cancer to diabetes to alzheimer’s.on the other hand, many people believe that this benefit to medicine comes at the costof potential human lives. if you want a bit of background on the moral and medical controversysurrounding stem cells, you can check out

either of these videos on screen. originally, the 14-day limit comes from a1979 united states department of health, education, and welfare report. a committee of theologians,psychologists, and doctors came to a compromise: human embryonic stem cells could be studiedfor two weeks after fertilization, beyond which time the cells would have to be destroyed.but this limit was fairly arbitrary, as at the time, scientists could not keep embryosalive in vitro for more than a few days. a later report, organized in 1984 by britishexistential philosopher mary warnock, justified the two week limit. the report states thaton the 14th or 15th day, a faint line of cells appears on the embryo, called the “primitivestreak”. this, it was argued, is a moment

that signifies that the embryo has becomean individual being, as before this time the embryo could potentially split into twin organisms. one of the reasons this stage appealed tothose who objected on moral grounds, was that if an embryo could split into two people,then it could not yet be an individual person. the rule codified an easy to measure mark,coupled with an unambiguous time frame; making the question less about conception or “asoul”, while still allowing for a religious and moral compromise. additionally, a 2002 report from californiastated that less than half of all fertilized embryos, both in vitro and in vivo, ever reachthe primitive streak, meaning that most of

embryos used for research would have beenunlikely to make it to term anyway.. but recent advances have made it possiblefor scientists to keep embryos alive for longer than two weeks, by simulating womb-like conditions.with the potential for further research using stem cells, the question has been forced again:is the 14-day limit still valid? some scientists say no. arguing that theycould use the research in preventing miscarriages, infertility, and birth defects which theybelieve to be more important than a more or less arbitrary time limit. for example, in2014, researchers were able to cure “induced parkinson's disease” in rats neuroscientistsused human embryonic stem cells to create neurons that produce dopamine, which is missingin those who suffer from the disease. although

no human clinical trials have been done, theseearly results with animals have been very promising. that said, other researchers in bioethicshave pointed out that even an arbitrary limit is better than no limit at all. as more restrictionsare lifted, the very real question becomes “where is the limit on human experimentationin the pursuit of knowledge?”

heart stem cell treatment

heart stem cell treatment

- they said roman hadhypoplastic left heart syndrome and the best thing that we could do would be to take him home and in probably about three or four days, he'dpass away on his own. i was 25 weeks pregnantwhen we went back home just absolutely devastatedand we decided to come to mayo and they gave us hope. (inspirational music) - the focus of this initialtrial is on the diagnosis of

hypoplastic left heart syndromeand that is a congenital heart defect where half of theheart is not really formed. now the ventricle that the childis left with is a ventricle that now has a muchbigger responsibility than what it was initiallydesigned for and so over time, the function of this ventriclegradually can get reduced to the point that the child,or maybe a young adult, will start to developsymptoms of heart failure. once the function ofthe ventricle goes down,

we don't have anythingthat we can do for that. stem cell therapy hasthe ability to improve the function of any of theseventricles that are failing. whether it be a child,whether it be an adult, whether it be a congenital defect, whether it be an adult defect. - the study here at mayo clinic with hypoplastic left heartchildren is really the first fda approved clinicaltrial using stem cells

to try to regenerate and curecongenital heart disease. the study is really designedto identify children with this disease before they're born, collect umbilical cord bloodat the time of their birth. these children typicallyneed three surgeries. first starting in thefirst few days of life, few months of life anda few years of life. these three open-heart surgeries give us an opportunity at thesecond one to deliver these

stem cells into their heartwith the intent of trying to make their heart bigger,better and stronger. roman went through theprocedure three months ago and received the stemcells and since that time, he's done extremely well. what we believe ishappening is these cells are probably stimulatingthe underlying regenerative capacity of the heart. there's 40,000 childrenborn in the united states

with congenital heartdisease and a good percentage of them develop heart failureso this type of therapy may allow us to delay or, ideally, prevent the need for cardiac transplantation. - i hope roman's future has no set-backs, nothing holds him back. - my hope for roman's surgeries is that it'll benefit people in the future. - the reality that we'refacing today in bio-medical

research is funding is being pushed down at the national level soit really creates this valley of death betweeninnovation and applications. - if you look at the majormilestones in medicine, we had antibiotic therapy for the life-threatening infections, then we had the inception of heart surgery using the heart lung machine. then we had transplantationwhere we were able

to come up with medicinesthat minimized rejection. that was probably the lastmajor miracle in medicine. this is the next potentialmiracle in medicine where it has the potentialto impact the largest number of patients in healthcare,in heart failure. so we can make a difference,so we should make a difference. thank you.

harvesting stem cells

harvesting stem cells

placidway is a leading medical tourism companythat helps you compare and customize the most affordable treatments worldwide.placidway, is a leader in medical travel. and helps people find the best package fortheir treatments. like with emily, she needed a bone marrowtransplant but she hadn't got enough money for the treatment. when she contacted placidwayshe learned that she can have affordable packages travelling abroad.so she chose the best bone marrow transplant package in hyderabad, india.by basavatarakam indo american cancer hospital & research institute.bone marrow transplant can be of two major types:1. when the patient’s own stem cells are

harvested and re infused after high-dose chemotherapy,it is called autologus bone marrow transplant. 2. when the stem cells are harvested fromhuman leukocyte antigen matched donor and infused to the patient after appropriate conditions,it is called allogenic bone marrow transplant. if you want to know more, contact us.subscribe to our you tube channel and get instant access to all of our latest medicalcare videos. enjoy your free pass to quality global healthcare!

harvard stem cell institute

harvard stem cell institute

the heart has very limited capacity for regenerationafter injury and this is an increase cause of uh human morbidity and mortality world wide there is a compelling un-clinical need toidentify the opposite cell type to drive robust cardiac muscle regeneration because this uh very recent ah discovery actuallyuh is the latest in a chain of scientific discoveries and for the first it uh reports ofthe identification

of the cell that could be viewed as perhapsan optimal cell type to promote cardiac muscle uh regeneration because the cells that have been isolatedhave come from embryonic stem cells and than had been used to form an intact stripfunctioning ventricular muscle tissue while you may start out with a very smallnumber of cells they have the capability

to proliferate and then maintain their ability to make muscle and it's that property that makes a very unique we decided to ask the question how is the heart built in the first placeif you want to rebuild a broken heart then go back and look at nature and findout how it's done normally so we went back to their embryo of mouse andwe essentially color coded the heart and were able to pick up very specific populations of hearts cellswhich have these unique qualities of being able to replicate

and at the same time being completely committedto the muscles heath aid the cells turn out to have it built in clocksin them meaning when we isolate them they are capableof of renewing for a while but then after a certain period of time they will stop reviewing and they would made sure into functioning my cartel tissue these are stem cells that are actually differentiating the test tube and from them working to generate the hearts tissue and using these cells and the tissue engineeringtechnology that was developed by a kit parker

and adam feinberg over in the school engineering we were able to generate two-dimensional mial cardial tissueout of that now to get to full cardiac regeneration weneed to get to the three dimensions but already we've taken this huge step forward with respectto regenerating the heart and we've develop a platform that will allow usto study how normal heart functions

haematopoietic stem cells

haematopoietic stem cells

numbness. when you first hear, you kind ofgo into this zone where the next thing you hear is your blood racing in your ears. wedid not know how much time i would have, so we needed to move quickly. here, at new york-presbyterian,their treatment plan had a very good chance of success, in fact they said, "you are agood possibility for a cure." those are the words you want to hear. new york-presbyterianhas been the number one hospital in new york for over 10 years now. we're able to treatevery kind of cancer that there is, and we're extremely proud of our bone marrow transplantprograms. on the weill cornell side, we have the bone marrow and hematopoietic stem celltransplantation program, while on the columbia side, we have our irving transplant unit.we pride ourselves on providing optimal care,

working closely with our colleagues, whileat the same time, moving the field and contributing to research. we offer the whole array of stemcell transplant procedures, which includes autologous transplants, allogeneic, from matchedsiblings, matched unrelated donors, or even half matched transplants, and offer a transplantoption to patients who otherwise don't have a fully matched donor. we did a worldwidesearch, we did it for months, but we didn't find an identical match, so the clinical trialwas my only option, and that was a technique that dr. van biesen perfected. we have thedoctors who actually make the discoveries that then take what's learned from the laband actually treat patients with it. we have all the latest technology, and we're innovativein terms of how we use that technology. it

was very important that this particular hospitaldoes the research that's necessary to assist the patient through the journey of a bonemarrow transplant. i like to go to the people who write the book, not the people that readthe book. a successful bone marrow transplant is a team effort. we work with amazing collaboratorshere at new york-presbyterian hospital. this is a multi-service hospital. when you undergoa stem cell transplant or a bone marrow transplant, you can get various complications. it's anamazing thing to have all these specialties, all with trainees, all with expertise, atyour site. they're telling you, "listen, this is our options, this is what we can do foryou." they always knew where i was in my progress and they were reporting back to me. everypatient is different and every patient deserves

individualized care, so we try as much aspossible to personalize the care that these patients receive, and we make sure that everypatient's goals and challenges are addressed appropriately. we have a motto here, whichsays, "we put patients first," and everything we do comes at it from the patient perspective.that's what really sets us apart. i knew i'd found a partner, i knew i found the rightplace, that's going to walk with me step by step to heal me.

fungsi stem cell

fungsi stem cell

flo hyman had always been a tall girl. i mean... really tall. by her 12th birthday, she was already six feet,and by 17 she’d topped out at just over 6’5’’. initially self-conscious about her stature,she learned to use it to her advantage when she started playing volleyball. she attended the university of houston asthe school’s first female scholarship athlete, and at the age of 21, she was competing inworld championships. nine years later she made it to the 1984 olympics and helped herteam win the silver medal. after the olympics, hyman moved to japan whereshe gained fame playing professional volleyball.

but all of that ended in 1986 when out ofnowhere, she collapsed and died during a game. she was 31 years old. hyman’s initial cause of death was thoughtto be a heart attack, but an autopsy revealed that she died from a tear in her aorta, caused by anundiagnosed condition known as marfan syndrome. marfan syndrome is a genetic disorder of theconnective tissue. people suffering from it have a defect in their connective tissue thatsubstantially weakens it over time. and you’ve got connective tissue pretty mucheverywhere in your body, so it can cause big problems. outwardly, those with marfan’s tend to tobe especially tall and thin, like flo hyman, with loose, flexible joints and noticeablylonger limbs and fingers.

those long fingers and bendy joints have actuallyhelped some athletes and musicians do things that the rest of us can’t -- famous blues guitaristrobert johnson, piano virtuoso sergei rachmaninov, and italian violinist niccolo paganini areall believed to have had marfan syndrome. but these abilities come at a great cost -- as peoplewith marfan’s get older, their weakening tissue can cause serious problems in the joints,eyes, lungs, and heart. the fact that a single genetic mutation canaffect your bones, cartilage, tendons, blood vessel walls, and more, shows that all ofthose structures are closely related, no matter how different they may seem. we’ve covered the basic properties of nervous,muscle, and epithelial tissue, but we haven’t

gotten to the most abundant and diverse ofthe four tissue types -- our connective tissue. this is the stuff that keeps you looking young,makes up your skeleton, and delivers oxygen and nutrients throughout your body. it’s whatholds you together, in more ways than one. and if something goes wrong with it, you’rein for some havoc. and that means we’re gonnabe talkin’ about jello today. uh…we’ll get to that in a minute. the springiness here? that’s connectivetissue. so is the structure in here, and the stuff inside here, and the tendons poppingout here connective tissue is pretty much everywherein your body, although how much of it shows

up where, varies from organ to organ. forinstance, your skin is mostly connective tissue, while your brain has very little, since it’salmost all nervous tissue. you’ve got four main classes of connectivetissue -- proper, or the kind you’d find in your ligaments and supporting your skin,along with cartilage, bone, and blood. whaaaa? sounds a little weird, but your bones andyour blood are just types of connective tissue! so, despite the name, your connective tissues do waymore than just connect your muscles to your bones. your fat -- which is a type of proper connectivetissue -- provides insulation and fuel storage -- whether you like it or not -- but it alsoserves structural purposes, like holding your

kidneys in place, and keeping your eyeballsfrom popping out of your skull. your bones, tendons, and cartilage bind, support,and protect your organs and give you a skeleton so that you can move with a purpose, insteadof blobbing around like an amoeba. and your blood transports your hormones, nutrients,and other material all over your body. there’s no other substance in you that can boast thiskind of diversity. but if they’re so different, how do we knowthat anything is a connective tissue? well, all connective tissues have three factors in commonthat set them apart from other tissue types. first, they share a common origin: they alldevelop from mesenchyme, a loose and fluid type of embryonic tissue. unlike the cellsthat go on to form, say, your epithelium,

which are fixed and neatly arranged in sheets,mesenchymal cells can be situated any-which-way, and can move from place to place. connective tissues also have different degreesof vascularity, or blood flow. most cartilage is avascular, for example, meaning it hasno blood vessels; while other types of connective tissue, like the dense irregular tissue inyour skin, is brimming with blood vessels. finally -- and as strange as it may sound-- all connective tissues are mostly composed of nonliving material, called the extracellularmatrix. while other tissue types are mainly made of living cells packed together, theinert matrix between connective-tissue cells is actually more important than what’s insidethe cells.

basically, your connective tissue, when yousee it up close, looks and acts a lot like this. yeah. the most abundant and diverse tissuein your body, that makes all of your movements and functions possible? turns out it’s notthat different from the dessert that aunt frances brings to every holiday party. the jello that gives this confection its structureis like that extracellular matrix in your connective tissue. the actual cells are justintermittent little goodies floating around inside the matrix -- like the little marshmallows. and although it may not look like it in thisparticular edible model, the extracellular matrix is mostly made of two components. themain part is the ground substance -- a watery,

rubbery, unstructured material that fillsin the spaces between cells, and -- like the gelatin in this dessert -- protects the delicate,delicious cells from their surroundings. the ground substance is flexible, becauseit’s mostly made of big ol’ starch and protein molecules mixed with water. the anchors of this framework are proteinscalled proteoglycans. and from each one sprouts lots and lots of long, starchy strands calledglycosaminoglycans, or gags, radiating out from those proteins like brush bristles. these molecules then clump together to formbig tangles that trap water, and if you’ve ever made glue out of flour, you know thatstarch, protein and water can make a strong

and gooey glue. but running throughout the ground substanceis another important component: fibers, which provide support and structure to the otherwiseshapeless ground substance. and here, too, are lots of different types. collagen is by far the strongest and mostabundant type of fiber. tough and flexible, it’s essentially a strand of protein, andstress tests show that it’s actually stronger than a steel fiber of the same size. it’spart of what makes your skin look young and plump, which is why sometimes we inject itinto our faces. in addition, you’ve also got elastic fibers-- which are longer and thinner, and form

a branching framework within the matrix. they’remade out of the protein elastin which allows them to stretch and recoil like rubber bands;they’re found in places like your skin, lungs, and blood vessel walls. finally, there are reticular fibers -- short,finer collagen fibers with an extra coating of glycoprotein. these fibers form delicate,sponge-like networks that cradle and support your organs like fuzzy nets. so, there’s ground substance and fibersin all connective tissue, but let’s not forget about the cells themselves. with a tissue as diverse as this, naturallythere are all kinds of connective tissue cells,

each with its unique and vital task -- frombuilding bone to storing energy to keeping you from bleeding to death every time youget a paper cut. but each of these signature cell types manifestsitself in two different phases: immature and mature. you can recognize the immature cells bythe suffix they all share in their names: -blast. “blast” sounds kinda destructive, butliterally it means “forming” -- these are the stem cells that are still in the processof dividing to replicate themselves. but each kind of blast cell has a specialized function:namely, to secrete the ground substances and fiber that form its unique matrix. so chondroblasts, for example, are the blastcells of cartilage. when they build their

matrix around them, they’re making the spongy tissuethat forms your nose and ears and cushions your joints. likewise, osteoblasts are the blast cellsof bone tissue, and the matrix they lay down is the nexus of calcium carbonate that formsyour bone. once they’re done forming their matrix, these blast cells transition intoa less active, mature phase. at that point, they trade in -blast for the suffix -cyte.so an osteoblast in your bone becomes an osteocyte -- ditto for chondroblasts becoming chondrocytes. these cyte cells maintain the health of thematrix built by the blasts, but they can sometimes revert back to their blast state if they needto repair or generate a new matrix. so, the matrices that these cells create arepretty much what build you -- they assemble

your bone and your cartilage and your tendonsand everything that holds the rest together. not bad for a bunch of marshmallows floatingin jello. but! there is another class of connectivetissue cells that are responsible for an equally important role. and that is: protecting you,from pretty much everything. these are cells that carry out many of yourbody’s immune functions. i’m talking about macrophages, the big,hungry guard cells that patrol your connective tissues and eat bacteria, foreign materials,and even your own dead cells. and your white blood cells, or leukocytesthat scour your circulatory system fighting off infection, they’re connective tissuecells, too.

you can see how pervasive and important connectivetissue is in your body. so a condition that affects this tissue, like marfan syndrome,can really wreak havoc. one of the best ways of understanding yourbody’s structures, after all, is studying what happens when something goes wrong withthem. in the case of your connective tissue, marfan syndrome affects those fibers we talkedabout, that lend structure and support to the extracellular matrix. most often, it targets the elastic fibers,causing weakness in the matrix that’s the root of many of the condition’s most serioussymptoms. about 90 percent of the people with the diseaseexperience problems with the heart and the

aorta -- the biggest and most important arteryin the body. when the elastic fibers around the aorta weaken, they can’t provide theartery with enough support. so, over time, the aorta begins to enlarge -- so much sothat it can rupture. this is probably what happened to flo hyman.she was physically exerting herself, and her artery -- without the support of its connectivetissue -- couldn’t take the stress, and it tore. there's so much going on with your connectivetissue -- so many variations within their weird diversity -- that we’re going to spendone last lesson on them next week, exploring the subtypes that come together to make youpossible. but you did learn a lot today! you learnedthat there are four types of connective tissue

-- proper, cartilage, bone, and blood -- andthat they all develop from mesenchyme, have different degrees of blood flow, and are mostlymade of extracellular matrix full of ground substance and fibers. we touched on differentblasts, and cyte, and immune cell types, and discussed how marfan syndrome can affect connectivetissue. thanks for watching, especially to our subbablesubscribers, who make crash course possible for themselves and also for the rest of theworld. to find out how you can become a supporter, just go to subbable.com. this episode was written by kathleen yale,edited by blake de pastino, and our consultant, is dr. brandon jackson. our director and editoris nicholas jenkins, the script supervisor

and sound designer is michael aranda, andthe graphics team is thought cafã©.

function of stem cells

function of stem cells

where we left off after themeiosis videos is that we had two gametes. we had a sperm and an egg. let me draw the sperm. so you had the sperm andthen you had an egg. maybe i'll do the egg ina different color. that's the egg, and we allknow how this story goes. the sperm fertilizes the egg. and a whole cascade of eventsstart occurring.

the walls of the egg then becomeimpervious to other sperm so that only one sperm canget in, but that's not the focus of this video. the focus of this video is howthis fertilized egg develops once it has become a zygote. so after it's fertilized, youremember from the meiosis videos that each of these werehaploid, or that they had-- oh, i added an extra i there--that they had half the contingency of the dna.

as soon as the sperm fertilizesthis egg, now, all of a sudden, you havea diploid zygote. let me do that. so now let me picka nice color. so now you're going to have adiploid zygote that's going to have a 2n complement of the dnamaterial or kind of the full complement of what a normalcell in our human body would have. so this is diploid,and it's a zygote, which is just a fancy way ofsaying the fertilized egg.

and it's now readyto essentially turn into an organism. so immediately afterfertilization, this zygote starts experiencing cleavage. it's experiencing mitosis,that's the mechanism, but it doesn't increasea lot in size. so this one right here will thenturn into-- it'll just split up via mitosisinto two like that. and, of course, these are each2n, and then those are going

to split into four like that. and each of these have the sameexact genetic complement as that first zygote, andit keeps splitting. and this mass of cells, we canstart calling it, this right here, this is referredto as the morula. and actually, it comes from theword for mulberry because it looks like a mulberry. so actually, let me just kindof simplify things a little bit because we don'thave to start here.

so we start with a zygote. this is a fertilized egg. it just starts duplicating viamitosis, and you end up with a ball of cells. it's often going to be a powerof two, because these cells, at least in the initial stagesare all duplicating all at once, and then youhave this morula. now, once the morula gets toabout 16 cells or so-- and we're talking aboutfour or five days.

this isn't an exact process--they started differentiating a little bit, where the outercells-- and this kind of turns into a sphere. let me make it a littlebit more sphere like. so it starts differentiatingbetween-- let me make some outer cells. this would be a cross-sectionof it. it's really going to lookmore like a sphere. that's the outer cells and thenyou have your inner cells

on the inside. these outer cells are calledthe trophoblasts. let me do it in adifferent color. let me scroll over. i don't want to go there. and then the inner cells, andthis is kind of the crux of what this video is allabout-- let me scroll down a little bit. the inner cells-- picka suitable color.

the inner cells right there arecalled the embryoblast. and then what's going to happenis some fluid's going to start filling in someof this gap between the embryoblast and the trophoblast,so you're going to start having some fluid thatcomes in there, and so the morula will eventuallylook like this, where the trophoblast, or the outermembrane, is kind of this huge sphere of cells. and this is all happening asthey keep replicating.

mitosis is the mechanism, so nowmy trophoblast is going to look like that, and thenmy embryoblast is going to look like this. sometimes the embryoblast-- sothis is the embryoblast. sometimes it's also called theinner cell mass, so let me write that. and this is what's going toturn into the organism. and so, just so you know acouple of the labels that are involved here, if we're dealingwith a mammalian

organism, and we are mammals,we call this thing that the morula turned into is a zygote,then a morula, then the cells of the morula startedto differentiate into the trophoblast, or kind of theoutside cells, and then the embryoblast. and then youhave this space that forms here, and this is just fluid,and it's called the blastocoel. a very non-intuitive spellingof the coel part of but once this is formed, this iscalled a blastocyst. that's

the entire thing right here. let me scroll downa little bit. this whole thing is called theblastocyst, and this is the case in humans. now, it can be a very confusingtopic, because a lot of times in a lot of books onbiology, you'll say, hey, you go from the morula tothe blastula or the blastosphere stage. let me write those words down.

so sometimes you'll say morula, and you go to blastula. sometimes it's calledthe blastosphere. and i want to make it veryclear that these are essentially the same stagesin development. these are just for-- you know,in a lot of books, they'll start talking about frogs ortadpoles or things like that, and this applies to them. while we're talking aboutmammals, especially the ones

that are closely relatedto us, the stage is the blastocyst stage, and the realdifferentiator is when people talk about just blastulaand blastospheres. there isn't necessarily thisdifferentiation between these outermost cells and theseembryonic, or this embryoblast, or this innercell mass here. but since the focus of thisvideo is humans, and really that's where i wanted to startfrom, because that's what we are and that's what'sinteresting, we're going to

focus on the blastocyst. now, everything i've talkedabout in this video, it was really to get to this point,because what we have here, these little green cells thati drew right here in the blastocysts, this inner cellmass, this is what will turn into the organism. and you say, ok, sal, if that'sthe organism, what's all of these purplecells out here? this trophoblast out there?

that is going to turn into theplacenta, and i'll do a future video where in a human, it'llturn into a placenta. so let me write that down. it'll turn into the placenta. and i'll do a whole future videoabout i guess how babies are born, and i actually learneda ton about that this past year because a babywas born in our house. but the placenta is reallykind of what the embryo develops inside of, and it's theinterface, especially in

humans and in mammals, betweenthe developing fetus and its mother, so it kind of is theexchange mechanism that separates their two systems,but allows the necessary functions to go onbetween them. but that's not the focusof this video. the focus of this video is thefact that these cells, which at this point are-- they'vedifferentiated themselves away from the placenta cells, butthey still haven't decided what they're going to become.

maybe this cell and itsdescendants eventually start becoming part of the nervoussystem, while these cells right here might become muscletissue, while these cells right here might becomethe liver. these cells right here arecalled embryonic stem cells, and probably the first time inthis video you're hearing a term that you might recognize. so if i were to just take one ofthese cells, and actually, just to introduce you to anotherterm, you know, we

have this zygote. as soon as it starts dividing,each of these cells are called a blastomere. and you're probably wondering,sal, why does this word blast keep appearing in this kindof embryology video, these development videos? and that comes from the greekfor spore: blastos. so the organism is beginningto spore out or grow. i won't go into the word originsof it, but that's

where it comes from and that'swhy everything has this blast in it. so these are blastomeres. so when i talk what embryonicstem cells, i'm talking about the individual blastomeresinside of this embryoblast or inside of this innercell mass. these words are actuallyunusually fun to say. so each of these is anembryonic stem cell. let me write this downin a vibrant color.

so each of these right here areembryonic stem cells, and i wanted to get to this. and the reason why these areinteresting, and i think you already know, is that there'sa huge debate around these. one, these have the potentialto turn into anything, that they have this plasticity. that's another word thatyou might hear. let me write that down,too: plasticity. and the word essentially comesfrom, you know, like a plastic

can turn into anything else. when we say that something hasplasticity, we're talking about its potentialto turn into a lot of different things. so the theory is, and there'salready some trials that seem to substantiate this, especiallyin some lower organisms, that, look, if youhave some damage at some point in your body-- let medraw a nerve cell. let me say i have a-- i won'tgo into the actual mechanics

of a nerve cell, but let's saythat we have some damage at some point on a nerve cell rightthere, and because of that, someone is paralyzedor there's some nerve dysfunction. we're dealing with multiplesclerosis or who knows what. the idea is, look, we have thesecell here that could turn into anything, and we'rejust really understanding how it knows what to turn into. it really has to look at itsenvironment and say, hey, what

are the guys around me doing,and maybe that's what helps dictate what it does. but the idea is you take thesethings that could turn to anything and you put them wherethe damage is, you layer them where the damage is, andthen they can turn into the cell that they needto turn into. so in this case, they wouldturn into nerve cells. they would turn to nerve cellsand repair the damage and maybe cure the paralysisfor that individual.

so it's a huge, exciting areaof research, and you could even, in theory, grownew organs. if someone needs a kidneytransplant or a heart transplant, maybe in the future,we could take a colony of these embryonic stem cells. maybe we can put them in sometype of other creature, or who knows what, and we can turn itinto a replacement heart or a replacement kidney. so there's a huge amountof excitement about

what these can do. i mean, they could cure a lot offormerly uncurable diseases or provide hope for alot of patients who might otherwise die. but obviously, there'sa debate here. and the debate all revolvesaround the issue of if you were to go in here and try toextract one of these cells, you're going to killthis embryo. you're going to kill thisdeveloping embryo, and that

developing embryo hadthe potential to become a human being. it's a potential that obviouslyhas to be in the right environment, and it hasto have a willing mother and all of the rest, but it doeshave the potential. and so for those, especially, ithink, in the pro-life camp, who say, hey, anything that hasa potential to be a human being, that is life and itshould not be killed. so people on that side of thecamp, they're against the

destroying of this embryo. i'm not making this video totake either side to that argument, but it's a potentialto turn to a human being. it's a potential, right? so obviously, there's a hugeamount of debate, but now, now you know in this video whatpeople are talking about when they say embryonic stem cells. and obviously, the next questionis, hey, well, why don't they just call them stemcells as opposed to embryonic

stem cells? and that's because in all of ourbodies, you do have what are called somatic stem cells. let me write that down. somatic or adults stem cells. and we all have them. they're in our bone marrow tohelp produce red blood cells, other parts of our body, but theproblem with somatic stem cells is they're not as plastic,which means that they

can't form any type of cellin the human body. there's an area of researchwhere people are actually maybe trying to make them moreplastic, and if they are able to take these somatic stemcells and make them more plastic, it might maybe killthe need to have these embryonic stem cells, althoughmaybe if they do this too good, maybe these will havethe potential to turn into human beings as well,so that could become a debatable issue.

but right now, this isn't anarea of debate because, left to their own devices, a somaticstem cell or an adult stem cell won't turn intoa human being, while an embryonic one, if it isimplanted in a willing mother, then, of course, it will turninto a human being. and i want to make one sidenote here, because i don't want to take any sides on thedebate of-- well, i mean, facts are facts. this does have the potentialto turn into a human being,

but it also has the potentialto save millions of lives. both of those statements arefacts, and then you can decide on your own which side of thatargument you'd like to or what side of that balance youwould like to kind of put your own opinion. but there's one thing i wantto talk about that in the public debate is neverbrought up. so you have this notion of whenyou-- to get an embryonic stem cell line, and when i saya stem cell line, i mean you

take a couple of stem cells, orlet's say you take one stem cell, and then you put it in apetri dish, and then you allow it to just duplicate. so this one turns into two,those two turn to four. then someone could take one ofthese and then put it in their own petri dish. these are a stem cell line. they all came from one uniqueembryonic stem cell or what initially was a blastomere.

so that's what they calla stem cell line. so the debate obviously is whenyou start an embryonic stem cell line, you aredestroying an embryo. but i want to make the pointhere that embryos are being destroyed in other processes,and namely, in-vitro fertilization. and maybe this'll be my nextvideo: fertilization. and this is just the notion thatthey take a set of eggs out of a mother.

it's usually a couple that'shaving trouble having a child, and they take a bunch ofeggs out of the mother. so let's say they takemaybe 10 to 30 eggs out of the mother. they actually perform a surgery,take them out of the ovaries of the mother, and thenthey fertilize them with semen, either it might comefrom the father or a sperm donor, so then all of thesebecomes zygotes once they're fertilized with semen.

so these all become zygotes,and then they allow them to develop, and they usually allowthem to develop to the blastocyst stage. so eventually all of theseturn into blastocysts. they have a blastocoel inthe center, which is this area of fluid. they have, of course, theembryo, the inner cell mass in them, and what they do is theylook at the ones that they deem are healthier or maybethe ones that are at least

just not unhealthy, and they'lltake a couple of these and they'll implant these intothe mother, so all of this is occurring in a petri dish. so maybe these four look good,so they're going to take these four, and they're going toimplant these into a mother, and if all goes well, maybe oneof these will turn into-- will give the couple a child. so this one will develop andmaybe the other ones won't. but if you've seen john & kateplus 8, you know that many

times they implant a lot ofthem in there, just to increase the probability thatyou get at least one child. but every now and then, theyimplant seven or eight, and then you end up witheight kids. and that's why in-vitrofertilization often results in kind of these multiplebirths, or reality television shows on cable. but what do they do with allof these other perfectly-- well, i won't say perfectlyviable, but these are embryos.

they may or may not be perfectlyviable, but you have these embryos that have thepotential, just like this one right here. these all have the potentialto turn into a human being. but most fertility clinics,roughly half of them, they either throw these away,they destroy them, they allow them to die. a lot of these are frozen, butjust the process of freezing them kills them and then bondingthem kills them again,

so most of these, the process ofin-vitro fertilization, for every one child that has thepotential to develop into a full-fledged human being, you'reactually destroying tens of very viable embryos. so at least my take on it isif you're against-- and i generally don't want to take aside on this, but if you are against research that involvesembryonic stem cells because of the destruction of embryos,on that same, i guess, philosophical ground, youshould also be against

in-vitro fertilization becauseboth of these involve the destruction of zygotes. i think-- well, i won't talkmore about this, because i really don't want to take sides,but i want to show that there is kind of an equivalencehere that's completely lost in this debateon whether embryonic stem cells should be used becausethey have a destruction of embryos, because you'redestroying just as many embryos in this-- well, i won'tsay just as many, but

you are destroying embryos. there's hundreds of thousands ofembryos that get destroyed and get frozen and obviouslydestroyed in that process as well through this in-vitrofertilization process. so anyway, now hopefully youhave the tools to kind of engage in the debate around stemcells, and you see that it all comes from what welearned about meiosis. they produce these gametes. the male gamete fertilizesa female gamete.

the zygote happens or getscreated and starts splitting up the morula, and then itkeeps splitting and it differentiates into theblastocyst, and then this is where the stem cells are. so you already know enoughscience to engage in kind of a very heated debate.