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Actomyosin meshwork mechanosensing enables tissue shape to orient cell force

Sculpting organism shape requires that cells produce forces with proper directionality. Thus, it is critical to understand how cells orient the cytoskeleton to produce forces that deform tissues. During Drosophila gastrulation, actomyosin contraction in ventral cells generates a long, narrow epithel...

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Autores principales: Chanet, Soline, Miller, Callie J., Vaishnav, Eeshit Dhaval, Ermentrout, Bard, Davidson, Lance A., Martin, Adam C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440693/
https://www.ncbi.nlm.nih.gov/pubmed/28504247
http://dx.doi.org/10.1038/ncomms15014
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author Chanet, Soline
Miller, Callie J.
Vaishnav, Eeshit Dhaval
Ermentrout, Bard
Davidson, Lance A.
Martin, Adam C.
author_facet Chanet, Soline
Miller, Callie J.
Vaishnav, Eeshit Dhaval
Ermentrout, Bard
Davidson, Lance A.
Martin, Adam C.
author_sort Chanet, Soline
collection PubMed
description Sculpting organism shape requires that cells produce forces with proper directionality. Thus, it is critical to understand how cells orient the cytoskeleton to produce forces that deform tissues. During Drosophila gastrulation, actomyosin contraction in ventral cells generates a long, narrow epithelial furrow, termed the ventral furrow, in which actomyosin fibres and tension are directed along the length of the furrow. Using a combination of genetic and mechanical perturbations that alter tissue shape, we demonstrate that geometrical and mechanical constraints act as cues to orient the cytoskeleton and tension during ventral furrow formation. We developed an in silico model of two-dimensional actomyosin meshwork contraction, demonstrating that actomyosin meshworks exhibit an inherent force orienting mechanism in response to mechanical constraints. Together, our in vivo and in silico data provide a framework for understanding how cells orient force generation, establishing a role for geometrical and mechanical patterning of force production in tissues.
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spelling pubmed-54406932017-06-02 Actomyosin meshwork mechanosensing enables tissue shape to orient cell force Chanet, Soline Miller, Callie J. Vaishnav, Eeshit Dhaval Ermentrout, Bard Davidson, Lance A. Martin, Adam C. Nat Commun Article Sculpting organism shape requires that cells produce forces with proper directionality. Thus, it is critical to understand how cells orient the cytoskeleton to produce forces that deform tissues. During Drosophila gastrulation, actomyosin contraction in ventral cells generates a long, narrow epithelial furrow, termed the ventral furrow, in which actomyosin fibres and tension are directed along the length of the furrow. Using a combination of genetic and mechanical perturbations that alter tissue shape, we demonstrate that geometrical and mechanical constraints act as cues to orient the cytoskeleton and tension during ventral furrow formation. We developed an in silico model of two-dimensional actomyosin meshwork contraction, demonstrating that actomyosin meshworks exhibit an inherent force orienting mechanism in response to mechanical constraints. Together, our in vivo and in silico data provide a framework for understanding how cells orient force generation, establishing a role for geometrical and mechanical patterning of force production in tissues. Nature Publishing Group 2017-05-15 /pmc/articles/PMC5440693/ /pubmed/28504247 http://dx.doi.org/10.1038/ncomms15014 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chanet, Soline
Miller, Callie J.
Vaishnav, Eeshit Dhaval
Ermentrout, Bard
Davidson, Lance A.
Martin, Adam C.
Actomyosin meshwork mechanosensing enables tissue shape to orient cell force
title Actomyosin meshwork mechanosensing enables tissue shape to orient cell force
title_full Actomyosin meshwork mechanosensing enables tissue shape to orient cell force
title_fullStr Actomyosin meshwork mechanosensing enables tissue shape to orient cell force
title_full_unstemmed Actomyosin meshwork mechanosensing enables tissue shape to orient cell force
title_short Actomyosin meshwork mechanosensing enables tissue shape to orient cell force
title_sort actomyosin meshwork mechanosensing enables tissue shape to orient cell force
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440693/
https://www.ncbi.nlm.nih.gov/pubmed/28504247
http://dx.doi.org/10.1038/ncomms15014
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