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Molecular Basis of Mammalian Embryonic Stem Cell Pluripotency and Self-Renewal

Mammalian embryonic stem cells (ESC) have a number of specific properties that make them a unique object of fundamental and applied studies. In culture, ESC can remain in an infinitely undifferentiated state and differentiate into descendants of all three germ layers – ectoderm, endoderm, and mesode...

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Detalles Bibliográficos
Autores principales: Medvedev, S.P., Shevchenko, A.I., Zakian, S.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: A.I. Gordeyev 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347565/
https://www.ncbi.nlm.nih.gov/pubmed/22649650
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author Medvedev, S.P.
Shevchenko, A.I.
Zakian, S.M.
author_facet Medvedev, S.P.
Shevchenko, A.I.
Zakian, S.M.
author_sort Medvedev, S.P.
collection PubMed
description Mammalian embryonic stem cells (ESC) have a number of specific properties that make them a unique object of fundamental and applied studies. In culture, ESC can remain in an infinitely undifferentiated state and differentiate into descendants of all three germ layers – ectoderm, endoderm, and mesoderm – that is, they can potentially produce more than 200 cell types comprising the body of an adult mammal. These properties of ESC are refered to as self-renewal and pluripotency. In this review, the basic signal pathways implicated in the maintenance of ESC pluripotency are considered. The major genes comprising a subsystem of “internal regulators of pluripotency,” their protein products and regulators, are characterized, and interaction with other factors is described as well. The role of epigenetic mechanisms and microRNAs in the system of ESC self-renewal and pluripotency, as well as the relationship between pluripotency and X-chromosome inactivation in female mammals, is discussed.
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spelling pubmed-33475652012-05-30 Molecular Basis of Mammalian Embryonic Stem Cell Pluripotency and Self-Renewal Medvedev, S.P. Shevchenko, A.I. Zakian, S.M. Acta Naturae Review Mammalian embryonic stem cells (ESC) have a number of specific properties that make them a unique object of fundamental and applied studies. In culture, ESC can remain in an infinitely undifferentiated state and differentiate into descendants of all three germ layers – ectoderm, endoderm, and mesoderm – that is, they can potentially produce more than 200 cell types comprising the body of an adult mammal. These properties of ESC are refered to as self-renewal and pluripotency. In this review, the basic signal pathways implicated in the maintenance of ESC pluripotency are considered. The major genes comprising a subsystem of “internal regulators of pluripotency,” their protein products and regulators, are characterized, and interaction with other factors is described as well. The role of epigenetic mechanisms and microRNAs in the system of ESC self-renewal and pluripotency, as well as the relationship between pluripotency and X-chromosome inactivation in female mammals, is discussed. A.I. Gordeyev 2010 /pmc/articles/PMC3347565/ /pubmed/22649650 Text en Copyright © 2010 Park-media Ltd. 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
Medvedev, S.P.
Shevchenko, A.I.
Zakian, S.M.
Molecular Basis of Mammalian Embryonic Stem Cell Pluripotency and Self-Renewal
title Molecular Basis of Mammalian Embryonic Stem Cell Pluripotency and Self-Renewal
title_full Molecular Basis of Mammalian Embryonic Stem Cell Pluripotency and Self-Renewal
title_fullStr Molecular Basis of Mammalian Embryonic Stem Cell Pluripotency and Self-Renewal
title_full_unstemmed Molecular Basis of Mammalian Embryonic Stem Cell Pluripotency and Self-Renewal
title_short Molecular Basis of Mammalian Embryonic Stem Cell Pluripotency and Self-Renewal
title_sort molecular basis of mammalian embryonic stem cell pluripotency and self-renewal
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347565/
https://www.ncbi.nlm.nih.gov/pubmed/22649650
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