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Cell reorientation under cyclic stretching

Mechanical cues from the extracellular microenvironment play a central role in regulating the structure, function and fate of living cells. Nevertheless, the precise nature of the mechanisms and processes underlying this crucial cellular mechanosensitivity remains a fundamental open problem. Here we...

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Detalles Bibliográficos
Autores principales: Livne, Ariel, Bouchbinder, Eran, Geiger, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066201/
https://www.ncbi.nlm.nih.gov/pubmed/24875391
http://dx.doi.org/10.1038/ncomms4938
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author Livne, Ariel
Bouchbinder, Eran
Geiger, Benjamin
author_facet Livne, Ariel
Bouchbinder, Eran
Geiger, Benjamin
author_sort Livne, Ariel
collection PubMed
description Mechanical cues from the extracellular microenvironment play a central role in regulating the structure, function and fate of living cells. Nevertheless, the precise nature of the mechanisms and processes underlying this crucial cellular mechanosensitivity remains a fundamental open problem. Here we provide a novel framework for addressing cellular sensitivity and response to external forces by experimentally and theoretically studying one of its most striking manifestations – cell reorientation to a uniform angle in response to cyclic stretching of the underlying substrate. We first show that existing approaches are incompatible with our extensive measurements of cell reorientation. We then propose a fundamentally new theory that shows that dissipative relaxation of the cell’s passively-stored, two-dimensional, elastic energy to its minimum actively drives the reorientation process. Our theory is in excellent quantitative agreement with the complete temporal reorientation dynamics of individual cells, measured over a wide range of experimental conditions, thus elucidating a basic aspect of mechanosensitivity.
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spelling pubmed-40662012014-11-30 Cell reorientation under cyclic stretching Livne, Ariel Bouchbinder, Eran Geiger, Benjamin Nat Commun Article Mechanical cues from the extracellular microenvironment play a central role in regulating the structure, function and fate of living cells. Nevertheless, the precise nature of the mechanisms and processes underlying this crucial cellular mechanosensitivity remains a fundamental open problem. Here we provide a novel framework for addressing cellular sensitivity and response to external forces by experimentally and theoretically studying one of its most striking manifestations – cell reorientation to a uniform angle in response to cyclic stretching of the underlying substrate. We first show that existing approaches are incompatible with our extensive measurements of cell reorientation. We then propose a fundamentally new theory that shows that dissipative relaxation of the cell’s passively-stored, two-dimensional, elastic energy to its minimum actively drives the reorientation process. Our theory is in excellent quantitative agreement with the complete temporal reorientation dynamics of individual cells, measured over a wide range of experimental conditions, thus elucidating a basic aspect of mechanosensitivity. 2014-05-30 /pmc/articles/PMC4066201/ /pubmed/24875391 http://dx.doi.org/10.1038/ncomms4938 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Livne, Ariel
Bouchbinder, Eran
Geiger, Benjamin
Cell reorientation under cyclic stretching
title Cell reorientation under cyclic stretching
title_full Cell reorientation under cyclic stretching
title_fullStr Cell reorientation under cyclic stretching
title_full_unstemmed Cell reorientation under cyclic stretching
title_short Cell reorientation under cyclic stretching
title_sort cell reorientation under cyclic stretching
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066201/
https://www.ncbi.nlm.nih.gov/pubmed/24875391
http://dx.doi.org/10.1038/ncomms4938
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