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Contact guidance persists under myosin inhibition due to the local alignment of adhesions and individual protrusions

Contact guidance—cell polarization by anisotropic substrate features—is integral to numerous physiological processes; however the complexities of its regulation are only beginning to be discovered. In particular, cells polarize to anisotropic features under non-muscle myosin II (MII) inhibition, des...

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Autores principales: Kubow, Kristopher E., Shuklis, Victoria D., Sales, Dominic J., Horwitz, A. Rick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662575/
https://www.ncbi.nlm.nih.gov/pubmed/29085052
http://dx.doi.org/10.1038/s41598-017-14745-7
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author Kubow, Kristopher E.
Shuklis, Victoria D.
Sales, Dominic J.
Horwitz, A. Rick
author_facet Kubow, Kristopher E.
Shuklis, Victoria D.
Sales, Dominic J.
Horwitz, A. Rick
author_sort Kubow, Kristopher E.
collection PubMed
description Contact guidance—cell polarization by anisotropic substrate features—is integral to numerous physiological processes; however the complexities of its regulation are only beginning to be discovered. In particular, cells polarize to anisotropic features under non-muscle myosin II (MII) inhibition, despite MII ordinarily being essential for polarized cell migration. Here, we investigate the ability of cells to sense and respond to fiber alignment in the absence of MII activity. We find that contact guidance is determined at the level of individual protrusions, which are individually guided by local fiber orientation, independent of MII. Protrusion stability and persistence are functions of adhesion lifetime, which depends on fiber orientation. Under MII inhibition, adhesion lifetime no longer depends on fiber orientation; however the ability of protrusions to form closely spaced adhesions sequentially without having to skip over gaps in adhesive area, biases protrusion formation along fibers. The co-alignment of multiple protrusions polarizes the entire cell; if the fibers are not aligned, contact guidance of individual protrusions still occurs, but does not produce overall cell polarization. These results describe how aligned features polarize a cell independently of MII and demonstrate how cellular contact guidance is built on the local alignment of adhesions and individual protrusions.
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spelling pubmed-56625752017-11-08 Contact guidance persists under myosin inhibition due to the local alignment of adhesions and individual protrusions Kubow, Kristopher E. Shuklis, Victoria D. Sales, Dominic J. Horwitz, A. Rick Sci Rep Article Contact guidance—cell polarization by anisotropic substrate features—is integral to numerous physiological processes; however the complexities of its regulation are only beginning to be discovered. In particular, cells polarize to anisotropic features under non-muscle myosin II (MII) inhibition, despite MII ordinarily being essential for polarized cell migration. Here, we investigate the ability of cells to sense and respond to fiber alignment in the absence of MII activity. We find that contact guidance is determined at the level of individual protrusions, which are individually guided by local fiber orientation, independent of MII. Protrusion stability and persistence are functions of adhesion lifetime, which depends on fiber orientation. Under MII inhibition, adhesion lifetime no longer depends on fiber orientation; however the ability of protrusions to form closely spaced adhesions sequentially without having to skip over gaps in adhesive area, biases protrusion formation along fibers. The co-alignment of multiple protrusions polarizes the entire cell; if the fibers are not aligned, contact guidance of individual protrusions still occurs, but does not produce overall cell polarization. These results describe how aligned features polarize a cell independently of MII and demonstrate how cellular contact guidance is built on the local alignment of adhesions and individual protrusions. Nature Publishing Group UK 2017-10-30 /pmc/articles/PMC5662575/ /pubmed/29085052 http://dx.doi.org/10.1038/s41598-017-14745-7 Text en © The Author(s) 2017 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
Kubow, Kristopher E.
Shuklis, Victoria D.
Sales, Dominic J.
Horwitz, A. Rick
Contact guidance persists under myosin inhibition due to the local alignment of adhesions and individual protrusions
title Contact guidance persists under myosin inhibition due to the local alignment of adhesions and individual protrusions
title_full Contact guidance persists under myosin inhibition due to the local alignment of adhesions and individual protrusions
title_fullStr Contact guidance persists under myosin inhibition due to the local alignment of adhesions and individual protrusions
title_full_unstemmed Contact guidance persists under myosin inhibition due to the local alignment of adhesions and individual protrusions
title_short Contact guidance persists under myosin inhibition due to the local alignment of adhesions and individual protrusions
title_sort contact guidance persists under myosin inhibition due to the local alignment of adhesions and individual protrusions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662575/
https://www.ncbi.nlm.nih.gov/pubmed/29085052
http://dx.doi.org/10.1038/s41598-017-14745-7
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