Screening the mammalian extracellular proteome for regulators of embryonic
human stem cell pluripotency.
«Human - mouse chimerism validates
human stem cell pluripotency» by Victoria L. Mascetti and Roger A. Pedersen published in Cell Stem Cell on Thursday 17 December 2015.
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.
The study, «VlincRNAs controlled by retroviral elements are a hallmark of
pluripotency and cancer» found that novel non-coding parts of the
human genome known as vlincRNAs (very long intergenic, non-coding RNAs) triggered by ancient viruses, participate in the biology of
stem cells, and in the development of cancer.
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.
Researchers describe how a microRNA can affect both
pluripotency and
cell cycle progression in
human pluripotent
stem cells
Human pluripotent
stem cells from two sources today, one physiological embryonic
stem cells «ES» from the embryo, and the other experimental
cells «iPS» induced
pluripotency by reprogramming genetic somatic
cells.
Loss of
pluripotency in
human embryonic
stem cells directly correlates with an increase in nuclear zinc.
«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.
«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.
His lab has pioneered the generation of clinical grade induced pluripotent
stem (iPS)
cells using non-viral reprogramming methods such as direct delivery of reprogrammed proteins and novel episomal methods, and has recently identified novel mechanisms underlying metabolic reprogramming during
human induced
pluripotency.
Reprogramming
human somatic
cells to
pluripotency represents a valuable resource for the development of in vitro based models for
human disease and holds tremendous potential for deriving patient - specific pluripotent
stem cells.
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.
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.
The pathways that connect expression of
stem cell surface glycoconjugates such as the TRA -1-60 / GCTM - 2 antigen, receptors, and growth factors in
human and even mouse ES
cells with the transcriptional networks that regulate
pluripotency remain unclear.
These two properties (self - renewal and
pluripotency) confers
human pluripotent
stem cells a unique interest for clinical applications since they could allow the production of infinite quantities of
cells for disease modelling, drug screening and
cell based therapy.