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Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion
Motile cells can use and switch between different modes of migration. Here, we use traction force microscopy and fluorescent labeling of actin and myosin to quantify and correlate traction force patterns and cytoskeletal distributions in Dictyostelium discoideum cells that move and switch between ke...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666840/ https://www.ncbi.nlm.nih.gov/pubmed/34898015 http://dx.doi.org/10.15252/msb.202110505 |
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author | Ghabache, Elisabeth Cao, Yuansheng Miao, Yuchuan Groisman, Alex Devreotes, Peter N Rappel, Wouter‐Jan |
author_facet | Ghabache, Elisabeth Cao, Yuansheng Miao, Yuchuan Groisman, Alex Devreotes, Peter N Rappel, Wouter‐Jan |
author_sort | Ghabache, Elisabeth |
collection | PubMed |
description | Motile cells can use and switch between different modes of migration. Here, we use traction force microscopy and fluorescent labeling of actin and myosin to quantify and correlate traction force patterns and cytoskeletal distributions in Dictyostelium discoideum cells that move and switch between keratocyte‐like fan‐shaped, oscillatory, and amoeboid modes. We find that the wave dynamics of the cytoskeletal components critically determine the traction force pattern, cell morphology, and migration mode. Furthermore, we find that fan‐shaped cells can exhibit two different propulsion mechanisms, each with a distinct traction force pattern. Finally, the traction force patterns can be recapitulated using a computational model, which uses the experimentally determined spatiotemporal distributions of actin and myosin forces and a viscous cytoskeletal network. Our results suggest that cell motion can be generated by friction between the flow of this network and the substrate. |
format | Online Article Text |
id | pubmed-8666840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86668402021-12-30 Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion Ghabache, Elisabeth Cao, Yuansheng Miao, Yuchuan Groisman, Alex Devreotes, Peter N Rappel, Wouter‐Jan Mol Syst Biol Articles Motile cells can use and switch between different modes of migration. Here, we use traction force microscopy and fluorescent labeling of actin and myosin to quantify and correlate traction force patterns and cytoskeletal distributions in Dictyostelium discoideum cells that move and switch between keratocyte‐like fan‐shaped, oscillatory, and amoeboid modes. We find that the wave dynamics of the cytoskeletal components critically determine the traction force pattern, cell morphology, and migration mode. Furthermore, we find that fan‐shaped cells can exhibit two different propulsion mechanisms, each with a distinct traction force pattern. Finally, the traction force patterns can be recapitulated using a computational model, which uses the experimentally determined spatiotemporal distributions of actin and myosin forces and a viscous cytoskeletal network. Our results suggest that cell motion can be generated by friction between the flow of this network and the substrate. John Wiley and Sons Inc. 2021-12-13 /pmc/articles/PMC8666840/ /pubmed/34898015 http://dx.doi.org/10.15252/msb.202110505 Text en © 2021 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Ghabache, Elisabeth Cao, Yuansheng Miao, Yuchuan Groisman, Alex Devreotes, Peter N Rappel, Wouter‐Jan Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion |
title | Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion |
title_full | Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion |
title_fullStr | Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion |
title_full_unstemmed | Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion |
title_short | Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion |
title_sort | coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666840/ https://www.ncbi.nlm.nih.gov/pubmed/34898015 http://dx.doi.org/10.15252/msb.202110505 |
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