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The biochemical composition of the actomyosin network sets the magnitude of cellular traction forces

The regulation of cellular force production relies on the complex interplay between a well-conserved set of proteins of the cytoskeleton: actin, myosin, and α-actinin. Despite our deep knowledge of the role of these proteins in force production at the molecular scale, our understanding of the bioche...

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Autores principales: Kollimada, Somanna, Senger, Fabrice, Vignaud, Timothée, Théry, Manuel, Blanchoin, Laurent, Kurzawa, Laëtitia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684728/
https://www.ncbi.nlm.nih.gov/pubmed/34410837
http://dx.doi.org/10.1091/mbc.E21-03-0109
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author Kollimada, Somanna
Senger, Fabrice
Vignaud, Timothée
Théry, Manuel
Blanchoin, Laurent
Kurzawa, Laëtitia
author_facet Kollimada, Somanna
Senger, Fabrice
Vignaud, Timothée
Théry, Manuel
Blanchoin, Laurent
Kurzawa, Laëtitia
author_sort Kollimada, Somanna
collection PubMed
description The regulation of cellular force production relies on the complex interplay between a well-conserved set of proteins of the cytoskeleton: actin, myosin, and α-actinin. Despite our deep knowledge of the role of these proteins in force production at the molecular scale, our understanding of the biochemical regulation of the magnitude of traction forces generated at the entire-cell level has been limited, notably by the technical challenge of measuring traction forces and the endogenous biochemical composition in the same cell. In this study, we developed an alternative Traction-Force Microscopy (TFM) assay, which used a combination of hydrogel micropatterning to define cell adhesion and shape and an intermediate fixation/immunolabeling step to characterize strain energies and the endogenous protein contents in single epithelial cells. Our results demonstrated that both the signal intensity and the area of the Focal Adhesion (FA)–associated protein vinculin showed a strong positive correlation with strain energy in mature FAs. Individual contents from actin filament and phospho-myosin displayed broader deviation in their linear relationship to strain energies. Instead, our quantitative analyzes demonstrated that their relative amount exhibited an optimum ratio of phospho-myosin to actin, allowing maximum force production by cells. By contrast, although no correlation was identified between individual α-actinin content and strain energy, the ratio of α-actinin to actin filaments was inversely related to strain energy. Hence, our results suggest that, in the cellular model studied, traction-force magnitude is dictated by the relative numbers of molecular motors and cross-linkers per actin filament, rather than the amounts of an individual component in the cytoskeletal network. This assay offers new perspectives to study in more detail the complex interplay between the endogenous biochemical composition of individual cells and the force they produce.
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spelling pubmed-86847282021-12-20 The biochemical composition of the actomyosin network sets the magnitude of cellular traction forces Kollimada, Somanna Senger, Fabrice Vignaud, Timothée Théry, Manuel Blanchoin, Laurent Kurzawa, Laëtitia Mol Biol Cell Articles The regulation of cellular force production relies on the complex interplay between a well-conserved set of proteins of the cytoskeleton: actin, myosin, and α-actinin. Despite our deep knowledge of the role of these proteins in force production at the molecular scale, our understanding of the biochemical regulation of the magnitude of traction forces generated at the entire-cell level has been limited, notably by the technical challenge of measuring traction forces and the endogenous biochemical composition in the same cell. In this study, we developed an alternative Traction-Force Microscopy (TFM) assay, which used a combination of hydrogel micropatterning to define cell adhesion and shape and an intermediate fixation/immunolabeling step to characterize strain energies and the endogenous protein contents in single epithelial cells. Our results demonstrated that both the signal intensity and the area of the Focal Adhesion (FA)–associated protein vinculin showed a strong positive correlation with strain energy in mature FAs. Individual contents from actin filament and phospho-myosin displayed broader deviation in their linear relationship to strain energies. Instead, our quantitative analyzes demonstrated that their relative amount exhibited an optimum ratio of phospho-myosin to actin, allowing maximum force production by cells. By contrast, although no correlation was identified between individual α-actinin content and strain energy, the ratio of α-actinin to actin filaments was inversely related to strain energy. Hence, our results suggest that, in the cellular model studied, traction-force magnitude is dictated by the relative numbers of molecular motors and cross-linkers per actin filament, rather than the amounts of an individual component in the cytoskeletal network. This assay offers new perspectives to study in more detail the complex interplay between the endogenous biochemical composition of individual cells and the force they produce. The American Society for Cell Biology 2021-08-19 /pmc/articles/PMC8684728/ /pubmed/34410837 http://dx.doi.org/10.1091/mbc.E21-03-0109 Text en © 2021 Kollimada et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.
spellingShingle Articles
Kollimada, Somanna
Senger, Fabrice
Vignaud, Timothée
Théry, Manuel
Blanchoin, Laurent
Kurzawa, Laëtitia
The biochemical composition of the actomyosin network sets the magnitude of cellular traction forces
title The biochemical composition of the actomyosin network sets the magnitude of cellular traction forces
title_full The biochemical composition of the actomyosin network sets the magnitude of cellular traction forces
title_fullStr The biochemical composition of the actomyosin network sets the magnitude of cellular traction forces
title_full_unstemmed The biochemical composition of the actomyosin network sets the magnitude of cellular traction forces
title_short The biochemical composition of the actomyosin network sets the magnitude of cellular traction forces
title_sort biochemical composition of the actomyosin network sets the magnitude of cellular traction forces
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684728/
https://www.ncbi.nlm.nih.gov/pubmed/34410837
http://dx.doi.org/10.1091/mbc.E21-03-0109
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