Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783238111434637312 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5440693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT chanetsoline actomyosinmeshworkmechanosensingenablestissueshapetoorientcellforce AT millercalliej actomyosinmeshworkmechanosensingenablestissueshapetoorientcellforce AT vaishnaveeshitdhaval actomyosinmeshworkmechanosensingenablestissueshapetoorientcellforce AT ermentroutbard actomyosinmeshworkmechanosensingenablestissueshapetoorientcellforce AT davidsonlancea actomyosinmeshworkmechanosensingenablestissueshapetoorientcellforce AT martinadamc actomyosinmeshworkmechanosensingenablestissueshapetoorientcellforce |