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Actomyosin contractility-dependent matrix stretch and recoil induces rapid cell migration
Cells select from a diverse repertoire of migration strategies. Recent developments in tunable biomaterials have helped identify how extracellular matrix properties influence migration, however, many settings lack the fibrous architecture characteristic of native tissues. To investigate migration in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414652/ https://www.ncbi.nlm.nih.gov/pubmed/30862791 http://dx.doi.org/10.1038/s41467-019-09121-0 |
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author | Wang, William Y. Davidson, Christopher D. Lin, Daphne Baker, Brendon M. |
author_facet | Wang, William Y. Davidson, Christopher D. Lin, Daphne Baker, Brendon M. |
author_sort | Wang, William Y. |
collection | PubMed |
description | Cells select from a diverse repertoire of migration strategies. Recent developments in tunable biomaterials have helped identify how extracellular matrix properties influence migration, however, many settings lack the fibrous architecture characteristic of native tissues. To investigate migration in fibrous contexts, we independently varied the alignment and stiffness of synthetic 3D fiber matrices and identified two phenotypically distinct migration modes. In contrast to stiff matrices where cells migrated continuously in a traditional mesenchymal fashion, cells in deformable matrices stretched matrix fibers to store elastic energy; subsequent adhesion failure triggered sudden matrix recoil and rapid cell translocation. Across a variety of cell types, traction force measurements revealed a relationship between cell contractility and the matrix stiffness where this migration mode occurred optimally. Given the prevalence of fibrous tissues, an understanding of how matrix structure and mechanics influences migration could improve strategies to recruit repair cells to wound sites or inhibit cancer metastasis. |
format | Online Article Text |
id | pubmed-6414652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64146522019-03-14 Actomyosin contractility-dependent matrix stretch and recoil induces rapid cell migration Wang, William Y. Davidson, Christopher D. Lin, Daphne Baker, Brendon M. Nat Commun Article Cells select from a diverse repertoire of migration strategies. Recent developments in tunable biomaterials have helped identify how extracellular matrix properties influence migration, however, many settings lack the fibrous architecture characteristic of native tissues. To investigate migration in fibrous contexts, we independently varied the alignment and stiffness of synthetic 3D fiber matrices and identified two phenotypically distinct migration modes. In contrast to stiff matrices where cells migrated continuously in a traditional mesenchymal fashion, cells in deformable matrices stretched matrix fibers to store elastic energy; subsequent adhesion failure triggered sudden matrix recoil and rapid cell translocation. Across a variety of cell types, traction force measurements revealed a relationship between cell contractility and the matrix stiffness where this migration mode occurred optimally. Given the prevalence of fibrous tissues, an understanding of how matrix structure and mechanics influences migration could improve strategies to recruit repair cells to wound sites or inhibit cancer metastasis. Nature Publishing Group UK 2019-03-12 /pmc/articles/PMC6414652/ /pubmed/30862791 http://dx.doi.org/10.1038/s41467-019-09121-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, William Y. Davidson, Christopher D. Lin, Daphne Baker, Brendon M. Actomyosin contractility-dependent matrix stretch and recoil induces rapid cell migration |
title | Actomyosin contractility-dependent matrix stretch and recoil induces rapid cell migration |
title_full | Actomyosin contractility-dependent matrix stretch and recoil induces rapid cell migration |
title_fullStr | Actomyosin contractility-dependent matrix stretch and recoil induces rapid cell migration |
title_full_unstemmed | Actomyosin contractility-dependent matrix stretch and recoil induces rapid cell migration |
title_short | Actomyosin contractility-dependent matrix stretch and recoil induces rapid cell migration |
title_sort | actomyosin contractility-dependent matrix stretch and recoil induces rapid cell migration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414652/ https://www.ncbi.nlm.nih.gov/pubmed/30862791 http://dx.doi.org/10.1038/s41467-019-09121-0 |
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