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Mechanics of the cellular microenvironment as probed by cells in vivo during zebrafish presomitic mesoderm differentiation

Tissue morphogenesis, homoeostasis and repair require cells to constantly monitor their three-dimensional microenvironment and adapt their behaviours in response to local biochemical and mechanical cues. Yet the mechanical parameters of the cellular microenvironment probed by cells in vivo remain un...

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Autores principales: Mongera, Alessandro, Pochitaloff, Marie, Gustafson, Hannah J., Stooke-Vaughan, Georgina A., Rowghanian, Payam, Kim, Sangwoo, Campàs, Otger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812792/
https://www.ncbi.nlm.nih.gov/pubmed/36577855
http://dx.doi.org/10.1038/s41563-022-01433-9
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author Mongera, Alessandro
Pochitaloff, Marie
Gustafson, Hannah J.
Stooke-Vaughan, Georgina A.
Rowghanian, Payam
Kim, Sangwoo
Campàs, Otger
author_facet Mongera, Alessandro
Pochitaloff, Marie
Gustafson, Hannah J.
Stooke-Vaughan, Georgina A.
Rowghanian, Payam
Kim, Sangwoo
Campàs, Otger
author_sort Mongera, Alessandro
collection PubMed
description Tissue morphogenesis, homoeostasis and repair require cells to constantly monitor their three-dimensional microenvironment and adapt their behaviours in response to local biochemical and mechanical cues. Yet the mechanical parameters of the cellular microenvironment probed by cells in vivo remain unclear. Here, we report the mechanics of the cellular microenvironment that cells probe in vivo and in situ during zebrafish presomitic mesoderm differentiation. By quantifying both endogenous cell-generated strains and tissue mechanics, we show that individual cells probe the stiffness associated with deformations of the supracellular, foam-like tissue architecture. Stress relaxation leads to a perceived microenvironment stiffness that decreases over time, with cells probing the softest regime. We find that most mechanical parameters, including those probed by cells, vary along the anteroposterior axis as mesodermal progenitors differentiate. These findings expand our understanding of in vivo mechanosensation and might aid the design of advanced scaffolds for tissue engineering applications.
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spelling pubmed-98127922023-01-06 Mechanics of the cellular microenvironment as probed by cells in vivo during zebrafish presomitic mesoderm differentiation Mongera, Alessandro Pochitaloff, Marie Gustafson, Hannah J. Stooke-Vaughan, Georgina A. Rowghanian, Payam Kim, Sangwoo Campàs, Otger Nat Mater Article Tissue morphogenesis, homoeostasis and repair require cells to constantly monitor their three-dimensional microenvironment and adapt their behaviours in response to local biochemical and mechanical cues. Yet the mechanical parameters of the cellular microenvironment probed by cells in vivo remain unclear. Here, we report the mechanics of the cellular microenvironment that cells probe in vivo and in situ during zebrafish presomitic mesoderm differentiation. By quantifying both endogenous cell-generated strains and tissue mechanics, we show that individual cells probe the stiffness associated with deformations of the supracellular, foam-like tissue architecture. Stress relaxation leads to a perceived microenvironment stiffness that decreases over time, with cells probing the softest regime. We find that most mechanical parameters, including those probed by cells, vary along the anteroposterior axis as mesodermal progenitors differentiate. These findings expand our understanding of in vivo mechanosensation and might aid the design of advanced scaffolds for tissue engineering applications. Nature Publishing Group UK 2022-12-28 2023 /pmc/articles/PMC9812792/ /pubmed/36577855 http://dx.doi.org/10.1038/s41563-022-01433-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mongera, Alessandro
Pochitaloff, Marie
Gustafson, Hannah J.
Stooke-Vaughan, Georgina A.
Rowghanian, Payam
Kim, Sangwoo
Campàs, Otger
Mechanics of the cellular microenvironment as probed by cells in vivo during zebrafish presomitic mesoderm differentiation
title Mechanics of the cellular microenvironment as probed by cells in vivo during zebrafish presomitic mesoderm differentiation
title_full Mechanics of the cellular microenvironment as probed by cells in vivo during zebrafish presomitic mesoderm differentiation
title_fullStr Mechanics of the cellular microenvironment as probed by cells in vivo during zebrafish presomitic mesoderm differentiation
title_full_unstemmed Mechanics of the cellular microenvironment as probed by cells in vivo during zebrafish presomitic mesoderm differentiation
title_short Mechanics of the cellular microenvironment as probed by cells in vivo during zebrafish presomitic mesoderm differentiation
title_sort mechanics of the cellular microenvironment as probed by cells in vivo during zebrafish presomitic mesoderm differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812792/
https://www.ncbi.nlm.nih.gov/pubmed/36577855
http://dx.doi.org/10.1038/s41563-022-01433-9
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