While the potential of adult stem cells has been understood for some time, researchers have argued that
the pluripotency of embryonic stem cells — their ability to be transformed into most if not all of the various cell types of the body — make them more valuable both for research and potentially someday for treatment.
Not exact matches
«Human
embryonic stem cells remain the gold standard for
pluripotency,» Francis Collins, director
of the National Institutes
of Health, said at the hearing.
Whitehead Institute researchers have determined that the transcription factor Nanog, which plays a critical role in the self - renewal
of embryonic stem cells, is expressed in a manner similar to other
pluripotency markers.
This gene is also known to help human
embryonic stem cells stay flexible enough to become any type
of body
cell, a property known as
pluripotency.
Pluripotency distinguishes
embryonic stem cells from adult
stem cells found in adults; while
embryonic stem cells can generate all
cell types in the body, adult
stem cells are multipotent and can produce only a limited number
of cell types.
Two papers claiming that stressing the body's
cell could produce
embryonic - like
stem cells, a process called stimulus - triggered acquisition
of pluripotency (STAP), were heralded when published in Nature in January but thrashed soon after when problematic images and figures were soon found.
Mouse
embryonic stem cells stained for key
pluripotency markersGRAZIANO MARTELLO Combining computer science algorithms with biological data has enabled researchers to create a model
of the minimal number
of factors necessary for mouse
embryonic stem cells (ESCs) to self - renew in culture.
Yamanaka and Takahashi began their search by studying
embryonic stem cells in the hope
of identifying the genes that underlie essential
stem cell characteristics, such as
pluripotency and proliferation, a
cell's ability to replicate itself.
A whole network
of these proteins is involved in giving
embryonic stem (ES)
cells pluripotency — the ability to generate all the
cell lineages
of the body.
Debojyoti Chakraborty (Buchholz, TUD)-- «Systematic dissection
of long non coding RNAs involved in the regulation
of embryonic stem cell pluripotency» (2014)
Loss
of pluripotency in human
embryonic stem cells directly correlates with an increase in nuclear zinc.
Title: Inhibition
of glycogen synthase kinase - 3 alleviates Tcf3 repression
of the
pluripotency network and increases
embryonic stem cell resistance to differentiation Authors: Wray J, Kalkan T, Gomez - Lopez S, Eckardt D, Cook A, Kemler R & Smith A Date: 19th June 2011 Publication Details: Nature Cell Biology 13,838 — 845 (2011) doi: 10.1038 / ncb
cell resistance to differentiation Authors: Wray J, Kalkan T, Gomez - Lopez S, Eckardt D, Cook A, Kemler R & Smith A Date: 19th June 2011 Publication Details: Nature
Cell Biology 13,838 — 845 (2011) doi: 10.1038 / ncb
Cell Biology 13,838 — 845 (2011) doi: 10.1038 / ncb2267
New research at the Hebrew University
of Jerusalem sheds light on
pluripotency — the ability
of embryonic stem cells to renew themselves...
«The current extension
of induced
pluripotency to human
cells is a major development and although it is early days for this technique it may well prove to be every bit as signifcant as the first derivation
of human
embryonic stem cells nine years ago.
A human
embryonic stem cell is reined in — prevented from giving up its unique characteristics
of self - renewal and
pluripotency — by the presence
of a protein modification that stifles any genes that would prematurely instruct the
cell to develop into heart or other specialized tissue.
iPSCs are
cells that were originally from adult tissues, but have been forced to produce proteins that are thought to be essential for the
pluripotency of human
embryonic stem cells.
Title: Nanog Variability and
Pluripotency Regulation
of Embryonic Stem Cells - Insights from a Mathematical Model Analysis Authors: Glauche I, Herberg M, Roeder I Date: June 2010 Publication Details: PLoS ONE 5 (6): e11238
But the eyebrow - raising reports claimed that adult
stem cells sometimes behave like their
embryonic counterparts, mimicking their trademark capacity to engender all types
of cells — an ability dubbed
pluripotency.
Studies in cultured
embryonic stem (ES)
cells, and our analysis
of zebrafish embryos have revealed that
pluripotency is characterized by a unique chromatin signature.
«This discovery will advance our understanding
of stem cell epigenetics and chromatin structures, provide potential mechanisms on maintaining the hallmark properties
of ES
cells, and help researchers with the rich source
of information to better understand some
of the unique features — such as self - renewal and
pluripotency —
of human
embryonic stem cells,» said Ng Huck Hui, Ph.D., senior group leader at GIS and a member
of the Singapore team that conducted this research.
Further, we demonstrate that deletion
of Alkbh1 in
embryonic stem cells leads to upregulation
of the core genes involved in
pluripotency and that ALKBH1 is required during early differentiation.
Topics covered include
embryonic stem cells,
pluripotency, germline
stem cells, tissue - specific
stem cells,
stem cell differentiation, epigenetics,
stem cell genomics and systems biology, genome reprogramming, cancer
stem cells,
stem cell niches,
stem -
cell - based disease models, nuclear transfer technology, bioengineering, drug discovery, in vivo imaging
of stem cells, therapeutic applications, regenerative medicine, clinical and translational insights,
stem cell research policies, ethical issues, and technical or resource - based innovations.
He seeks to understand the molecular mechanisms that underlie
pluripotency and the rapid proliferation
of embryonic stem cells — they can become any type
of cell in the body — and to identify the factors that induce reprogramming.
Embryonic stem cells derived from human blastocysts have the key advantage
of pluripotency, meaning that they form nearly all
cell types but also have the disadvantage
of forming tumors in vivo, which may limit clinical application to tissue engineering rather than
cell transplantation.
Writing in the journal
Cell Stem Cell, the team reports that more than half of mouse epiblast stem cells treated with the drug reversed course within three days, and regained an embryonic «be anything» state, also called pluripote
Stem Cell, the team reports that more than half
of mouse epiblast
stem cells treated with the drug reversed course within three days, and regained an embryonic «be anything» state, also called pluripote
stem cells treated with the drug reversed course within three days, and regained an
embryonic «be anything» state, also called
pluripotency.
Correlation
of expression and methylation
of imprinted genes with
pluripotency of parthenogenetic
embryonic stem cells
Screening the mammalian extracellular proteome for regulators
of embryonic human
stem cell pluripotency.
Citation: Hough SR, Laslett AL, Grimmond SB, Kolle G, Pera MF (2009) A Continuum
of Cell States Spans
Pluripotency and Lineage Commitment in Human
Embryonic Stem Cells.
An important concept in this research is
pluripotency ---- the ability
of the human
embryonic stem cell to differentiate or become almost any
cell in the body, explained senior author Kenneth S. Kosik, professor in the Department
of Molecular, Cellular & Developmental Biology (MCDB).
Currently,
stem cell research focuses on renewal and differentiation
of stem cells and the molecular mechanisms
of its
pluripotency - or their ability to develop into any type
of cell - using human
embryonic stem cells, induced pluripotent
stem cells, and
stem cells in simpler organisms.
Execution
of pluripotency requires progression from the naïve status represented by mouse
embryonic stem cells (ESCs) to a state capacitated for lineage specification.
Studies have identified transcription factors such as Stat3, Nanog, and Oct4 as being necessary for
embryonic stem (ES)
cell self - renewal and maintenance
of pluripotency.