Cargando…

Effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin–paxillin recruitment at single focal adhesions

Focal adhesions (FAs) regulate force transfer between the cytoskeleton and ECM–integrin complexes. We previously showed that vinculin regulates force transmission at FAs. Vinculin residence time in FAs correlated with applied force, supporting a mechanosensitive model in which forces stabilize vincu...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Dennis W., Lee, Ted T., Weng, Shinuo, Fu, Jianping, García, Andrés J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541841/
https://www.ncbi.nlm.nih.gov/pubmed/28468976
http://dx.doi.org/10.1091/mbc.E17-02-0116
_version_ 1783254889693970432
author Zhou, Dennis W.
Lee, Ted T.
Weng, Shinuo
Fu, Jianping
García, Andrés J.
author_facet Zhou, Dennis W.
Lee, Ted T.
Weng, Shinuo
Fu, Jianping
García, Andrés J.
author_sort Zhou, Dennis W.
collection PubMed
description Focal adhesions (FAs) regulate force transfer between the cytoskeleton and ECM–integrin complexes. We previously showed that vinculin regulates force transmission at FAs. Vinculin residence time in FAs correlated with applied force, supporting a mechanosensitive model in which forces stabilize vinculin’s active conformation to promote force transfer. In the present study, we examined the relationship between traction force and vinculin–paxillin localization to single FAs in the context of substrate stiffness and actomyosin contractility. We found that vinculin and paxillin FA area did not correlate with traction force magnitudes at single FAs, and this was consistent across different ECM stiffness and cytoskeletal tension states. However, vinculin residence time at FAs varied linearly with applied force for stiff substrates, and this was disrupted on soft substrates and after contractility inhibition. In contrast, paxillin residence time at FAs was independent of local applied force and substrate stiffness. Paxillin recruitment and residence time at FAs, however, were dependent on cytoskeletal contractility on lower substrate stiffness values. Finally, substrate stiffness and cytoskeletal contractility regulated whether vinculin and paxillin turnover dynamics are correlated to each other at single FAs. This analysis sheds new insights on the coupling among force, substrate stiffness, and FA dynamics.
format Online
Article
Text
id pubmed-5541841
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher The American Society for Cell Biology
record_format MEDLINE/PubMed
spelling pubmed-55418412017-09-22 Effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin–paxillin recruitment at single focal adhesions Zhou, Dennis W. Lee, Ted T. Weng, Shinuo Fu, Jianping García, Andrés J. Mol Biol Cell Articles Focal adhesions (FAs) regulate force transfer between the cytoskeleton and ECM–integrin complexes. We previously showed that vinculin regulates force transmission at FAs. Vinculin residence time in FAs correlated with applied force, supporting a mechanosensitive model in which forces stabilize vinculin’s active conformation to promote force transfer. In the present study, we examined the relationship between traction force and vinculin–paxillin localization to single FAs in the context of substrate stiffness and actomyosin contractility. We found that vinculin and paxillin FA area did not correlate with traction force magnitudes at single FAs, and this was consistent across different ECM stiffness and cytoskeletal tension states. However, vinculin residence time at FAs varied linearly with applied force for stiff substrates, and this was disrupted on soft substrates and after contractility inhibition. In contrast, paxillin residence time at FAs was independent of local applied force and substrate stiffness. Paxillin recruitment and residence time at FAs, however, were dependent on cytoskeletal contractility on lower substrate stiffness values. Finally, substrate stiffness and cytoskeletal contractility regulated whether vinculin and paxillin turnover dynamics are correlated to each other at single FAs. This analysis sheds new insights on the coupling among force, substrate stiffness, and FA dynamics. The American Society for Cell Biology 2017-07-07 /pmc/articles/PMC5541841/ /pubmed/28468976 http://dx.doi.org/10.1091/mbc.E17-02-0116 Text en © 2017 Zhou et al. 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 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Zhou, Dennis W.
Lee, Ted T.
Weng, Shinuo
Fu, Jianping
García, Andrés J.
Effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin–paxillin recruitment at single focal adhesions
title Effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin–paxillin recruitment at single focal adhesions
title_full Effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin–paxillin recruitment at single focal adhesions
title_fullStr Effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin–paxillin recruitment at single focal adhesions
title_full_unstemmed Effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin–paxillin recruitment at single focal adhesions
title_short Effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin–paxillin recruitment at single focal adhesions
title_sort effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin–paxillin recruitment at single focal adhesions
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541841/
https://www.ncbi.nlm.nih.gov/pubmed/28468976
http://dx.doi.org/10.1091/mbc.E17-02-0116
work_keys_str_mv AT zhoudennisw effectsofsubstratestiffnessandactomyosincontractilityoncouplingbetweenforcetransmissionandvinculinpaxillinrecruitmentatsinglefocaladhesions
AT leetedt effectsofsubstratestiffnessandactomyosincontractilityoncouplingbetweenforcetransmissionandvinculinpaxillinrecruitmentatsinglefocaladhesions
AT wengshinuo effectsofsubstratestiffnessandactomyosincontractilityoncouplingbetweenforcetransmissionandvinculinpaxillinrecruitmentatsinglefocaladhesions
AT fujianping effectsofsubstratestiffnessandactomyosincontractilityoncouplingbetweenforcetransmissionandvinculinpaxillinrecruitmentatsinglefocaladhesions
AT garciaandresj effectsofsubstratestiffnessandactomyosincontractilityoncouplingbetweenforcetransmissionandvinculinpaxillinrecruitmentatsinglefocaladhesions