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A mechanistic motor-clutch model that explains cell shape dynamics to cyclic stretch

Many cells in the body experience cyclic mechanical loading, which can impact cellular processes and morphology. In vitro studies often report that cells reorient in response to cyclic stretch of their substrate. To explore cellular mechanisms involved in this reorientation, a computational model wa...

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Autores principales: Scandling, Benjamin W., Gou, Jia, Thomas, Jessica, Xuan, Jacqueline, Xue, Chuan, Gooch, Keith J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250388/
https://www.ncbi.nlm.nih.gov/pubmed/35020463
http://dx.doi.org/10.1091/mbc.E20-01-0087
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author Scandling, Benjamin W.
Gou, Jia
Thomas, Jessica
Xuan, Jacqueline
Xue, Chuan
Gooch, Keith J.
author_facet Scandling, Benjamin W.
Gou, Jia
Thomas, Jessica
Xuan, Jacqueline
Xue, Chuan
Gooch, Keith J.
author_sort Scandling, Benjamin W.
collection PubMed
description Many cells in the body experience cyclic mechanical loading, which can impact cellular processes and morphology. In vitro studies often report that cells reorient in response to cyclic stretch of their substrate. To explore cellular mechanisms involved in this reorientation, a computational model was developed by adapting previous computational models of the actin–myosin–integrin motor-clutch system developed by others. The computational model predicts that under most conditions, actin bundles align perpendicular to the direction of applied cyclic stretch, but under specific conditions, such as low substrate stiffness, actin bundles align parallel to the direction of stretch. The model also predicts that stretch frequency impacts the rate of reorientation and that proper myosin function is critical in the reorientation response. These computational predictions are consistent with reports from the literature and new experimental results presented here. The model suggests that the impact of different stretching conditions (stretch type, amplitude, frequency, substrate stiffness, etc.) on the direction of cell alignment can largely be understood by considering their impact on cell–substrate detachment events, specifically whether detachments preferentially occur during stretching or relaxing of the substrate.
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spelling pubmed-92503882022-07-07 A mechanistic motor-clutch model that explains cell shape dynamics to cyclic stretch Scandling, Benjamin W. Gou, Jia Thomas, Jessica Xuan, Jacqueline Xue, Chuan Gooch, Keith J. Mol Biol Cell Articles Many cells in the body experience cyclic mechanical loading, which can impact cellular processes and morphology. In vitro studies often report that cells reorient in response to cyclic stretch of their substrate. To explore cellular mechanisms involved in this reorientation, a computational model was developed by adapting previous computational models of the actin–myosin–integrin motor-clutch system developed by others. The computational model predicts that under most conditions, actin bundles align perpendicular to the direction of applied cyclic stretch, but under specific conditions, such as low substrate stiffness, actin bundles align parallel to the direction of stretch. The model also predicts that stretch frequency impacts the rate of reorientation and that proper myosin function is critical in the reorientation response. These computational predictions are consistent with reports from the literature and new experimental results presented here. The model suggests that the impact of different stretching conditions (stretch type, amplitude, frequency, substrate stiffness, etc.) on the direction of cell alignment can largely be understood by considering their impact on cell–substrate detachment events, specifically whether detachments preferentially occur during stretching or relaxing of the substrate. The American Society for Cell Biology 2022-02-18 /pmc/articles/PMC9250388/ /pubmed/35020463 http://dx.doi.org/10.1091/mbc.E20-01-0087 Text en © 2022 Scandling, Gou, 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/4.0/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 4.0 International Creative Commons License.
spellingShingle Articles
Scandling, Benjamin W.
Gou, Jia
Thomas, Jessica
Xuan, Jacqueline
Xue, Chuan
Gooch, Keith J.
A mechanistic motor-clutch model that explains cell shape dynamics to cyclic stretch
title A mechanistic motor-clutch model that explains cell shape dynamics to cyclic stretch
title_full A mechanistic motor-clutch model that explains cell shape dynamics to cyclic stretch
title_fullStr A mechanistic motor-clutch model that explains cell shape dynamics to cyclic stretch
title_full_unstemmed A mechanistic motor-clutch model that explains cell shape dynamics to cyclic stretch
title_short A mechanistic motor-clutch model that explains cell shape dynamics to cyclic stretch
title_sort mechanistic motor-clutch model that explains cell shape dynamics to cyclic stretch
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250388/
https://www.ncbi.nlm.nih.gov/pubmed/35020463
http://dx.doi.org/10.1091/mbc.E20-01-0087
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