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Nanog Dynamics in Mouse Embryonic Stem Cells: Results from Systems Biology Approaches

Mouse embryonic stem cells (mESCs), derived from the inner cell mass of the blastocyst, are pluripotent stem cells having self-renewal capability and the potential of differentiating into every cell type under the appropriate culture conditions. An increasing number of reports have been published to...

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Detalles Bibliográficos
Autor principal: Marucci, Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480057/
https://www.ncbi.nlm.nih.gov/pubmed/28684962
http://dx.doi.org/10.1155/2017/7160419
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author Marucci, Lucia
author_facet Marucci, Lucia
author_sort Marucci, Lucia
collection PubMed
description Mouse embryonic stem cells (mESCs), derived from the inner cell mass of the blastocyst, are pluripotent stem cells having self-renewal capability and the potential of differentiating into every cell type under the appropriate culture conditions. An increasing number of reports have been published to uncover the molecular mechanisms that orchestrate pluripotency and cell fate specification using combined computational and experimental methodologies. Here, we review recent systems biology approaches to describe the causes and functions of gene expression heterogeneity and complex temporal dynamics of pluripotency markers in mESCs under uniform culture conditions. In particular, we focus on the dynamics of Nanog, a key regulator of the core pluripotency network and of mESC fate. We summarize the strengths and limitations of different experimental and modeling approaches and discuss how various strategies could be used.
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spelling pubmed-54800572017-07-06 Nanog Dynamics in Mouse Embryonic Stem Cells: Results from Systems Biology Approaches Marucci, Lucia Stem Cells Int Review Article Mouse embryonic stem cells (mESCs), derived from the inner cell mass of the blastocyst, are pluripotent stem cells having self-renewal capability and the potential of differentiating into every cell type under the appropriate culture conditions. An increasing number of reports have been published to uncover the molecular mechanisms that orchestrate pluripotency and cell fate specification using combined computational and experimental methodologies. Here, we review recent systems biology approaches to describe the causes and functions of gene expression heterogeneity and complex temporal dynamics of pluripotency markers in mESCs under uniform culture conditions. In particular, we focus on the dynamics of Nanog, a key regulator of the core pluripotency network and of mESC fate. We summarize the strengths and limitations of different experimental and modeling approaches and discuss how various strategies could be used. Hindawi 2017 2017-06-08 /pmc/articles/PMC5480057/ /pubmed/28684962 http://dx.doi.org/10.1155/2017/7160419 Text en Copyright © 2017 Lucia Marucci. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under 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
Marucci, Lucia
Nanog Dynamics in Mouse Embryonic Stem Cells: Results from Systems Biology Approaches
title Nanog Dynamics in Mouse Embryonic Stem Cells: Results from Systems Biology Approaches
title_full Nanog Dynamics in Mouse Embryonic Stem Cells: Results from Systems Biology Approaches
title_fullStr Nanog Dynamics in Mouse Embryonic Stem Cells: Results from Systems Biology Approaches
title_full_unstemmed Nanog Dynamics in Mouse Embryonic Stem Cells: Results from Systems Biology Approaches
title_short Nanog Dynamics in Mouse Embryonic Stem Cells: Results from Systems Biology Approaches
title_sort nanog dynamics in mouse embryonic stem cells: results from systems biology approaches
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480057/
https://www.ncbi.nlm.nih.gov/pubmed/28684962
http://dx.doi.org/10.1155/2017/7160419
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