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Membrane Tension Gates ERK-Mediated Regulation of Pluripotent Cell Fate
Cell fate transitions are frequently accompanied by changes in cell shape and mechanics. However, how cellular mechanics affects the instructive signaling pathways controlling cell fate is poorly understood. To probe the interplay between shape, mechanics, and fate, we use mouse embryonic stem cells...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7875115/ https://www.ncbi.nlm.nih.gov/pubmed/33217323 http://dx.doi.org/10.1016/j.stem.2020.10.018 |
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author | De Belly, Henry Stubb, Aki Yanagida, Ayaka Labouesse, Céline Jones, Philip H. Paluch, Ewa K. Chalut, Kevin J. |
author_facet | De Belly, Henry Stubb, Aki Yanagida, Ayaka Labouesse, Céline Jones, Philip H. Paluch, Ewa K. Chalut, Kevin J. |
author_sort | De Belly, Henry |
collection | PubMed |
description | Cell fate transitions are frequently accompanied by changes in cell shape and mechanics. However, how cellular mechanics affects the instructive signaling pathways controlling cell fate is poorly understood. To probe the interplay between shape, mechanics, and fate, we use mouse embryonic stem cells (ESCs), which change shape as they undergo early differentiation. We find that shape change is regulated by a β-catenin-mediated decrease in RhoA activity and subsequent decrease in the plasma membrane tension. Strikingly, preventing a decrease in membrane tension results in early differentiation defects in ESCs and gastruloids. Decreased membrane tension facilitates the endocytosis of FGF signaling components, which activate ERK signaling and direct the exit from the ESC state. Increasing Rab5a-facilitated endocytosis rescues defective early differentiation. Thus, we show that a mechanically triggered increase in endocytosis regulates early differentiation. Our findings are of fundamental importance for understanding how cell mechanics regulates biochemical signaling and therefore cell fate. |
format | Online Article Text |
id | pubmed-7875115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-78751152021-02-18 Membrane Tension Gates ERK-Mediated Regulation of Pluripotent Cell Fate De Belly, Henry Stubb, Aki Yanagida, Ayaka Labouesse, Céline Jones, Philip H. Paluch, Ewa K. Chalut, Kevin J. Cell Stem Cell Article Cell fate transitions are frequently accompanied by changes in cell shape and mechanics. However, how cellular mechanics affects the instructive signaling pathways controlling cell fate is poorly understood. To probe the interplay between shape, mechanics, and fate, we use mouse embryonic stem cells (ESCs), which change shape as they undergo early differentiation. We find that shape change is regulated by a β-catenin-mediated decrease in RhoA activity and subsequent decrease in the plasma membrane tension. Strikingly, preventing a decrease in membrane tension results in early differentiation defects in ESCs and gastruloids. Decreased membrane tension facilitates the endocytosis of FGF signaling components, which activate ERK signaling and direct the exit from the ESC state. Increasing Rab5a-facilitated endocytosis rescues defective early differentiation. Thus, we show that a mechanically triggered increase in endocytosis regulates early differentiation. Our findings are of fundamental importance for understanding how cell mechanics regulates biochemical signaling and therefore cell fate. Cell Press 2021-02-04 /pmc/articles/PMC7875115/ /pubmed/33217323 http://dx.doi.org/10.1016/j.stem.2020.10.018 Text en © 2020 The Author(s) 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 | Article De Belly, Henry Stubb, Aki Yanagida, Ayaka Labouesse, Céline Jones, Philip H. Paluch, Ewa K. Chalut, Kevin J. Membrane Tension Gates ERK-Mediated Regulation of Pluripotent Cell Fate |
title | Membrane Tension Gates ERK-Mediated Regulation of Pluripotent Cell Fate |
title_full | Membrane Tension Gates ERK-Mediated Regulation of Pluripotent Cell Fate |
title_fullStr | Membrane Tension Gates ERK-Mediated Regulation of Pluripotent Cell Fate |
title_full_unstemmed | Membrane Tension Gates ERK-Mediated Regulation of Pluripotent Cell Fate |
title_short | Membrane Tension Gates ERK-Mediated Regulation of Pluripotent Cell Fate |
title_sort | membrane tension gates erk-mediated regulation of pluripotent cell fate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7875115/ https://www.ncbi.nlm.nih.gov/pubmed/33217323 http://dx.doi.org/10.1016/j.stem.2020.10.018 |
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