Pluripotent stem cells are the most potent type of stem cells; they have the ability to
differentiate into any human cell type and to reproduce indefinitely.
Not exact matches
How else can microscopic
cells evolve and
differentiate into a fully formed
human?
Stem
cells have also been identified in
human milk, and have the potential to
differentiate into mammary epithelial lineages under mammary differentiation conditions in vitro, as well as other
cell types in corresponding microenvironments, including bone
cells, brain
cells, liver
cells, pancreatic beta
cells and heart
cells.
Scientists headed by Dr. Stevens Rehen
differentiated human induced pluripotent stem (iPS)
cells into neural stem
cells and
into further complex tridimensional structures, known as neurospheres and brain organoids.
As it can take weeks to grow
human cells into intact
differentiated and functional tissues within Organ Chips, such as those that mimic the lung and intestine, and researchers seek to understand how drugs, toxins or other perturbations alter tissue structure and function, the team at the Wyss Institute for Biologically Inspired Engineering led by Donald Ingber has been searching for ways to non-invasively monitor the health and maturity of
cells cultured within these microfluidic devices over extended times.
Tufts University biomedical engineers recently published the first report of a promising new way to induce
human mesenchymal stem
cells (or hMSCs, which are derived from bone marrow) to
differentiate into neuron - like
cells: treating them with exosomes.
One likely reason for this is that animals undergo cellular differentiation;
human life begins as a single
cell that
differentiates into the various
cell types needed for different organs, body parts, blood, the immune system, etc..
The results obtained by Afsaneh Gaillard's team and that Pierre Vanderhaeghen at the Institute of Interdisciplinary Research in
Human and Molecular Biology show, for the first time, using mice, that pluripotent stem
cells differentiated into cortical neurons make it possible to reestablish damaged adult cortical circuits, both neuroanatomically and functionally.
Now, scientists at Boston University's Center for Regenerative Medicine (CReM) have announced two major findings that further our understanding of this process: the ability to grow and purify the earliest lung progenitors that emerge from
human stem
cells, and the ability to
differentiate these
cells into tiny «bronchospheres» that model cystic fibrosis.
But with
humans, she is using iPS
cells and has been working to develop the correct protocols to induce her stem
cells to
differentiate into different kinds of lung tissue.
Finally, they demonstrated that zebrafish OPCs
differentiate into mature oligodendrocytes when cultured together with
human motor neurons,
differentiated from induced pluripotent stem
cells.
- Our results provide new insights
into the mechanisms of how POLR3G gene regulates stem
cell state, which in turn sheds light on the complex mechanisms with which
human embryonic stem
cells both self - renew and maintain the ability to
differentiate.
Adult organisms ranging from fruit flies to
humans harbor adult stem
cells, some of which renew themselves through
cell division while others
differentiate into the specialized
cells needed to replace worn - out or damaged organs and tissues.
While stem
cells —
cells that have the potential to
differentiate into other types of
cells — exist in adult
humans, the most useful stem
cells are those found in embryos, which are pluripotent, capable of becoming nearly any
cell in the body.
During embryonic development, organ - specific
cell types are formed from pluripotent stem
cells, which can
differentiate into all
cell types of the
human body.
«Our focus here has been on early heart development, but the basic principles of patterning of
human pluripotent stem
cells, and subsequently
differentiating them, can be readily expanded
into a broad range of tissues for understanding embryogenesis and tissue morphogenesis,» said Healy.
They found that the model's stem
cells differentiate (specialize)
into the various
cells of the brain in the same way that they do in the first trimester of
human development.
Recent research by neuroscientist Fred Gage and colleagues at the University of California (UC), San Diego, has shown that one of the most common types of jumping gene in people, called L1, is particularly abundant in
human stem
cells in the brain that ultimately
differentiate into neurons and plays an important role in regulating neuronal development and proliferation.
RIKEN researchers have taken up this challenge, and the work published in
Cell Reports details how sequentially applying several signaling molecules to three - dimensional cultures of
human embryotic stem
cells prompts the
cells to
differentiate into functioning cerebellar neurons that self - organize to form the proper dorsal / ventral patterning and multi-layer structure found in the natural developing cerebellum.
Using a process called cellular reprogramming, the researchers take a patient's skin
cells, convert them
into so - called induced pluripotent stem (iPS)
cells, which can
differentiate into all the
cells within the
human body.
«Our focus here has been on early heart development, but the basic principles of patterning of
human pluripotent stem
cells, and subsequently
differentiating them, can be readily expanded
into a broad range of tissues for understanding embryogenesis and tissue morphogenesis,» said Dr. Healy.
«The region selective - state of these stem
cells is entirely novel for laboratory - cultured stem
cells and offers important insight
into how
human stem
cells might be
differentiated into derivatives that give rise to a wide range of tissues and organs,» says Jun Wu, a postdoctoral researcher in Izpisua Belmonte's lab and first author of the new paper.
Lamba and colleagues recently demonstrated that
human embryonic stem
cells could be directed to
differentiate into photoreceptors and respond to a light stimulus as measured by ERG in crx − / − mice (a model for Leber's congenital amaurosis)[5].
«ViaCyte was the first to
differentiate human stem
cells into glucose - responsive, insulin - producing
cells, and now we are running the first and only clinical trials of stem
cell - derived islet replacement therapies for type 1 diabetes,» said Paul Laikind, PhD, President and CEO of ViaCyte.
In the paper, published May 6, 2015 in Nature, the scientists report using these new stem
cells to develop the first reliable method for integrating
human stem
cells into nonviable mouse embryos in a laboratory dish in such a way that the
human cells began to
differentiate into early - stage tissues.
Presently,
human pluripotent stem
cells (hPSCs) are the most powerful cellular resource to challenge this complete reassessment of the scientific bases and goals of toxicity testing, since they present a unique opportunity to develop a wide variety of
human cell - based physiological test systems because they may be expanded indefinitely and triggered to
differentiate into any
cell type, offering additionally the possibility to represent the
human population diversity.
Human ES
cells treated with Noggin, Dickkopf - 1, and Insulin - like Growth Factor - 1 proteins
differentiate into functional photoreceptors [5].
They have already shown that they can transform
human fibroblast
cells into pluripotent stem
cells, and now plan to start working on delivering the proteins needed to
differentiate stem
cells into specialized tissues.
Here we show that it is feasible to
differentiate and mature
human embryonic stem
cells (hESCs)
into functional -LSB-...]
Typically, this involves creating a «scaffold» of natural or synthetic materials, seeding it with
human stem
cells that can
differentiate themselves
into particular tissue types, and providing the
cells with nutrients and a physical environment that encourages them to take on the three - dimensional structures and functions of a particular body part.
Human mesenchymal stem
cells (hMSCs) are currently the most common adult stem
cell type used for
cell therapy applications due to their regenerative properties and ability to
differentiate into multiple
cell lineages (adipocyte, chondro ¬ cyte, and osteocyte).
The group recently produced data showing that stem
cells from
human hair follicles also
differentiate into contractile smooth muscle
cells.
Unlike other
cell types, stem
cells are unspecialized
cells uniquely capable of making copies of themselves (self - renewing),
differentiating into specialized
cell types, and helping to maintain some tissues in the
human body.
He and colleagues have also succeeded in
differentiating human pluripotent stem
cells into retinal (RPE)
cells, and has shown that they provide long - term benefit in animal models of vision loss.
If they were permanent, ES
cells would never be able to
differentiate into heart, kidney, brain, bone, skin and the other specialize
cells crucial to normal
human functioning.
A trial being conducted by Advanced
Cell Technology is testing the effectiveness of MA09 - hRPE,
human ESCs terminally
differentiated into retinal pigment epithelial (RPE)
cells, in treating degenerative macular diseases.
Researchers at UCSB were able to make these
human iPS
cells differentiate, or turn
into, retinal
cells.
The self - renewable capacity of these
cells, their ability to
differentiate into several tissue progenitors (neural, mesenchymal stem
cells...), and the possibility to work with mutated
cell lines define
human stem
cells as a good basis for screening compounds libraries in order to discover new potential drugs for monogenic diseases.
To do this,
human stem
cell lines could be treated to
differentiate into human heart
cells in a dish.
Researchers have shown that
human induced pluripotent stem
cells can
differentiate and self - organize
into cardiac microchambers when spatially confined.
We have recently developed the use of site - specific nucleases to genetically engineer
human pluripotent stem
cells, which can be maintained indefinitely and
differentiated into any
cell type of interest.
The Herlyn lab is
differentiating multi-potent stem
cells from the
human dermis and reprogrammed stem
cells into melanocytes to test the hypothesis that melanocyte stem
cells are more prone to transformation than fully
differentiated cells, and that neighboring
cells and matrix in the microenvironment play critical roles in differentiation and transformation.
Furthermore,
human NSC - derived pluripotent stem
cells can
differentiate into all three germ lineages both in vitro and in vivo.
In a study using
human muscle tissue, scientists in Children's Stem
Cell Research Center - led by Johnny Huard, PhD, and Bruno Péault, PhD - isolated and characterized stem cells taken from blood vessels (known as myoendothelial cells) that are easily isolated using cell - sorting techniques, proliferate rapidly and can be differentiated in the laboratory into muscle, bone and cartilage ce
Cell Research Center - led by Johnny Huard, PhD, and Bruno Péault, PhD - isolated and characterized stem
cells taken from blood vessels (known as myoendothelial
cells) that are easily isolated using
cell - sorting techniques, proliferate rapidly and can be differentiated in the laboratory into muscle, bone and cartilage ce
cell - sorting techniques, proliferate rapidly and can be
differentiated in the laboratory
into muscle, bone and cartilage
cells.
Through extensive examination, we have shown that
human NSC - derived iPS
cells are phenotypically identical to hESCs by all pluripotential markers analyzed and for their ability to
differentiate into all three major germ lineages.
Human embryonic stem
cells differentiate into a homogeneous population of natural killer
cells with potent in vivo antitumor activity.
Stem
cells have the capacity to
differentiate into any of the different tissues making up the
human body, thus holding the promise of treating or curing diseases such as multiple sclerosis or spinal - cord injury by replacing diseased
cells with healthy
cells.
Following this, they demonstrated that neural progenitors from embryonic stem
cells could
differentiate themselves
into neurons in rat brains presenting lesions similar to those observed in
humans.
Saxena, Pratik, et al. «A programmable synthetic lineage - control network that
differentiates human IPSCs
into glucose - sensitive insulin - secreting beta - like
cells.»
Finally, we used this approach to encapsulate
human Neural Stem
Cells (hNSC) derived from
human Induced Pluripotent Stem
Cells (hIPSC), which were further
differentiated into neurons within the capsules with negligible loss of viability.