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Pressure and curvature control of the cell cycle in epithelia growing under spherical confinement

Morphogenesis requires spatiotemporal regulation of proliferation, both by biochemical and mechanical cues. In epithelia, this regulation is called contact inhibition of proliferation, but disentangling biochemical from mechanical cues remains challenging. Here, we show that epithelia growing under...

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Autores principales: Di Meglio, Ilaria, Trushko, Anastasiya, Guillamat, Pau, Blanch-Mercader, Carles, Abuhattum, Shada, Roux, Aurélien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433880/
https://www.ncbi.nlm.nih.gov/pubmed/36001958
http://dx.doi.org/10.1016/j.celrep.2022.111227
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author Di Meglio, Ilaria
Trushko, Anastasiya
Guillamat, Pau
Blanch-Mercader, Carles
Abuhattum, Shada
Roux, Aurélien
author_facet Di Meglio, Ilaria
Trushko, Anastasiya
Guillamat, Pau
Blanch-Mercader, Carles
Abuhattum, Shada
Roux, Aurélien
author_sort Di Meglio, Ilaria
collection PubMed
description Morphogenesis requires spatiotemporal regulation of proliferation, both by biochemical and mechanical cues. In epithelia, this regulation is called contact inhibition of proliferation, but disentangling biochemical from mechanical cues remains challenging. Here, we show that epithelia growing under confinement accumulate pressure that inhibits proliferation above a threshold value. During growth, epithelia spontaneously buckle, and cell proliferation is transiently reactivated within the fold. Reactivation of proliferation within folds correlated with the local reactivation of the mechano-sensing YAP/TAZ pathway. At late time points, when the pressure is highest, β-catenin activity increases. The threshold pressure increases when β-catenin is overactivated and decreases when β-catenin is inhibited. Altogether, our results suggest that different mechanical cues resulting from pressure inhibition of proliferation are at play through different mechano-sensing pathways: the β-catenin pathway sustains cell division under high pressure, and the YAP pathway senses local curvature.
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spelling pubmed-94338802022-09-08 Pressure and curvature control of the cell cycle in epithelia growing under spherical confinement Di Meglio, Ilaria Trushko, Anastasiya Guillamat, Pau Blanch-Mercader, Carles Abuhattum, Shada Roux, Aurélien Cell Rep Report Morphogenesis requires spatiotemporal regulation of proliferation, both by biochemical and mechanical cues. In epithelia, this regulation is called contact inhibition of proliferation, but disentangling biochemical from mechanical cues remains challenging. Here, we show that epithelia growing under confinement accumulate pressure that inhibits proliferation above a threshold value. During growth, epithelia spontaneously buckle, and cell proliferation is transiently reactivated within the fold. Reactivation of proliferation within folds correlated with the local reactivation of the mechano-sensing YAP/TAZ pathway. At late time points, when the pressure is highest, β-catenin activity increases. The threshold pressure increases when β-catenin is overactivated and decreases when β-catenin is inhibited. Altogether, our results suggest that different mechanical cues resulting from pressure inhibition of proliferation are at play through different mechano-sensing pathways: the β-catenin pathway sustains cell division under high pressure, and the YAP pathway senses local curvature. Cell Press 2022-08-23 /pmc/articles/PMC9433880/ /pubmed/36001958 http://dx.doi.org/10.1016/j.celrep.2022.111227 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Report
Di Meglio, Ilaria
Trushko, Anastasiya
Guillamat, Pau
Blanch-Mercader, Carles
Abuhattum, Shada
Roux, Aurélien
Pressure and curvature control of the cell cycle in epithelia growing under spherical confinement
title Pressure and curvature control of the cell cycle in epithelia growing under spherical confinement
title_full Pressure and curvature control of the cell cycle in epithelia growing under spherical confinement
title_fullStr Pressure and curvature control of the cell cycle in epithelia growing under spherical confinement
title_full_unstemmed Pressure and curvature control of the cell cycle in epithelia growing under spherical confinement
title_short Pressure and curvature control of the cell cycle in epithelia growing under spherical confinement
title_sort pressure and curvature control of the cell cycle in epithelia growing under spherical confinement
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433880/
https://www.ncbi.nlm.nih.gov/pubmed/36001958
http://dx.doi.org/10.1016/j.celrep.2022.111227
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