| Literature DB >> 33217323 |
Henry De Belly1, Aki Stubb2, Ayaka Yanagida3, Céline Labouesse4, Philip H Jones5, Ewa K Paluch6, Kevin J Chalut7.
Abstract
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.Entities:
Keywords: Beta-catenin; Cell fate choice; Cell surface mechanics; ERK; Embryonic stem cells; Endocytosis; Membrane tension; mechanical signalling; pluripotency
Mesh:
Year: 2020 PMID: 33217323 PMCID: PMC7875115 DOI: 10.1016/j.stem.2020.10.018
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633