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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2022
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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. |
format | Online Article Text |
id | pubmed-9250388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
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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