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The cell cycle and pluripotency

PSCs (pluripotent stem cells) possess two key properties that have made them the focus of global research efforts in regenerative medicine: they have unlimited expansion potential under conditions which favour their preservation as PSCs and they have the ability to generate all somatic cell types up...

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Detalles Bibliográficos
Autores principales: Hindley, Christopher, Philpott, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631102/
https://www.ncbi.nlm.nih.gov/pubmed/23535166
http://dx.doi.org/10.1042/BJ20121627
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author Hindley, Christopher
Philpott, Anna
author_facet Hindley, Christopher
Philpott, Anna
author_sort Hindley, Christopher
collection PubMed
description PSCs (pluripotent stem cells) possess two key properties that have made them the focus of global research efforts in regenerative medicine: they have unlimited expansion potential under conditions which favour their preservation as PSCs and they have the ability to generate all somatic cell types upon differentiation (pluripotency). Conditions have been defined in vitro in which pluripotency is maintained, or else differentiation is favoured and is directed towards specific somatic cell types. However, an unanswered question is whether or not the core cell cycle machinery directly regulates the pluripotency and differentiation properties of PSCs. If so, then manipulation of the cell cycle may represent an additional tool by which in vitro maintenance or differentiation of PSCs may be controlled in regenerative medicine. The present review aims to summarize our current understanding of links between the core cell cycle machinery and the maintenance of pluripotency in ESCs (embryonic stem cells) and iPSCs (induced PSCs).
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spelling pubmed-36311022013-04-25 The cell cycle and pluripotency Hindley, Christopher Philpott, Anna Biochem J Review Article PSCs (pluripotent stem cells) possess two key properties that have made them the focus of global research efforts in regenerative medicine: they have unlimited expansion potential under conditions which favour their preservation as PSCs and they have the ability to generate all somatic cell types upon differentiation (pluripotency). Conditions have been defined in vitro in which pluripotency is maintained, or else differentiation is favoured and is directed towards specific somatic cell types. However, an unanswered question is whether or not the core cell cycle machinery directly regulates the pluripotency and differentiation properties of PSCs. If so, then manipulation of the cell cycle may represent an additional tool by which in vitro maintenance or differentiation of PSCs may be controlled in regenerative medicine. The present review aims to summarize our current understanding of links between the core cell cycle machinery and the maintenance of pluripotency in ESCs (embryonic stem cells) and iPSCs (induced PSCs). Portland Press Ltd. 2013-03-28 2013-04-15 /pmc/articles/PMC3631102/ /pubmed/23535166 http://dx.doi.org/10.1042/BJ20121627 Text en © 2013 The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Licence (CC-BY)(http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hindley, Christopher
Philpott, Anna
The cell cycle and pluripotency
title The cell cycle and pluripotency
title_full The cell cycle and pluripotency
title_fullStr The cell cycle and pluripotency
title_full_unstemmed The cell cycle and pluripotency
title_short The cell cycle and pluripotency
title_sort cell cycle and pluripotency
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631102/
https://www.ncbi.nlm.nih.gov/pubmed/23535166
http://dx.doi.org/10.1042/BJ20121627
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