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Towards understanding the roles of position and geometry on cell fate decisions during preimplantation development

The first lineage segregation event in mouse embryos produces two separate cell populations: inner cell mass and trophectoderm. This is understood to be brought about by cells sensing their position within the embryo and differentiating accordingly. The cellular and molecular underpinnings of this p...

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Autores principales: Biggins, John S., Royer, Christophe, Watanabe, Tomoko, Srinivas, Shankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683091/
https://www.ncbi.nlm.nih.gov/pubmed/26349030
http://dx.doi.org/10.1016/j.semcdb.2015.09.006
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author Biggins, John S.
Royer, Christophe
Watanabe, Tomoko
Srinivas, Shankar
author_facet Biggins, John S.
Royer, Christophe
Watanabe, Tomoko
Srinivas, Shankar
author_sort Biggins, John S.
collection PubMed
description The first lineage segregation event in mouse embryos produces two separate cell populations: inner cell mass and trophectoderm. This is understood to be brought about by cells sensing their position within the embryo and differentiating accordingly. The cellular and molecular underpinnings of this process remain under investigation and have variously been considered to be completely stochastic or alternately, subject to some predisposition set up at fertilisation or before. Here, we consider these views in light of recent publications, discuss the possible role of cell geometry and mechanical forces in this process and describe how modelling could contribute in addressing this issue.
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spelling pubmed-46830912016-01-11 Towards understanding the roles of position and geometry on cell fate decisions during preimplantation development Biggins, John S. Royer, Christophe Watanabe, Tomoko Srinivas, Shankar Semin Cell Dev Biol Review The first lineage segregation event in mouse embryos produces two separate cell populations: inner cell mass and trophectoderm. This is understood to be brought about by cells sensing their position within the embryo and differentiating accordingly. The cellular and molecular underpinnings of this process remain under investigation and have variously been considered to be completely stochastic or alternately, subject to some predisposition set up at fertilisation or before. Here, we consider these views in light of recent publications, discuss the possible role of cell geometry and mechanical forces in this process and describe how modelling could contribute in addressing this issue. Academic Press 2015-12 /pmc/articles/PMC4683091/ /pubmed/26349030 http://dx.doi.org/10.1016/j.semcdb.2015.09.006 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Biggins, John S.
Royer, Christophe
Watanabe, Tomoko
Srinivas, Shankar
Towards understanding the roles of position and geometry on cell fate decisions during preimplantation development
title Towards understanding the roles of position and geometry on cell fate decisions during preimplantation development
title_full Towards understanding the roles of position and geometry on cell fate decisions during preimplantation development
title_fullStr Towards understanding the roles of position and geometry on cell fate decisions during preimplantation development
title_full_unstemmed Towards understanding the roles of position and geometry on cell fate decisions during preimplantation development
title_short Towards understanding the roles of position and geometry on cell fate decisions during preimplantation development
title_sort towards understanding the roles of position and geometry on cell fate decisions during preimplantation development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683091/
https://www.ncbi.nlm.nih.gov/pubmed/26349030
http://dx.doi.org/10.1016/j.semcdb.2015.09.006
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