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Fibrillar adhesion dynamics govern the timescales of nuclear mechano-response via the vimentin cytoskeleton
The cell nucleus is continuously exposed to external signals, of both chemical and mechanical nature. To ensure proper cellular response, cells need to regulate not only the transmission of these signals, but also their timing and duration. Such timescale regulation is well described for fluctuating...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10659263/ https://www.ncbi.nlm.nih.gov/pubmed/37986921 http://dx.doi.org/10.1101/2023.11.08.566191 |
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author | Beedle, Amy E.M. Jaganathan, Anuja Albajar-Sigalés, Aina Yavitt, F. Max Bera, Kaustav Andreu, Ion Granero-Moya, Ignasi Zalvidea, Dobryna Kechagia, Zanetta Wiche, Gerhard Trepat, Xavier Ivaska, Johanna Anseth, Kristi S. Shenoy, Vivek B. Roca-Cusachs, Pere |
author_facet | Beedle, Amy E.M. Jaganathan, Anuja Albajar-Sigalés, Aina Yavitt, F. Max Bera, Kaustav Andreu, Ion Granero-Moya, Ignasi Zalvidea, Dobryna Kechagia, Zanetta Wiche, Gerhard Trepat, Xavier Ivaska, Johanna Anseth, Kristi S. Shenoy, Vivek B. Roca-Cusachs, Pere |
author_sort | Beedle, Amy E.M. |
collection | PubMed |
description | The cell nucleus is continuously exposed to external signals, of both chemical and mechanical nature. To ensure proper cellular response, cells need to regulate not only the transmission of these signals, but also their timing and duration. Such timescale regulation is well described for fluctuating chemical signals, but if and how it applies to mechanical signals reaching the nucleus is still unknown. Here we demonstrate that the formation of fibrillar adhesions locks the nucleus in a mechanically deformed conformation, setting the mechanical response timescale to that of fibrillar adhesion remodelling (~1 hour). This process encompasses both mechanical deformation and associated mechanotransduction (such as via YAP), in response to both increased and decreased mechanical stimulation. The underlying mechanism is the anchoring of the vimentin cytoskeleton to fibrillar adhesions and the extracellular matrix through plectin 1f, which maintains nuclear deformation. Our results reveal a mechanism to regulate the timescale of mechanical adaptation, effectively setting a low pass filter to mechanotransduction. |
format | Online Article Text |
id | pubmed-10659263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106592632023-11-20 Fibrillar adhesion dynamics govern the timescales of nuclear mechano-response via the vimentin cytoskeleton Beedle, Amy E.M. Jaganathan, Anuja Albajar-Sigalés, Aina Yavitt, F. Max Bera, Kaustav Andreu, Ion Granero-Moya, Ignasi Zalvidea, Dobryna Kechagia, Zanetta Wiche, Gerhard Trepat, Xavier Ivaska, Johanna Anseth, Kristi S. Shenoy, Vivek B. Roca-Cusachs, Pere bioRxiv Article The cell nucleus is continuously exposed to external signals, of both chemical and mechanical nature. To ensure proper cellular response, cells need to regulate not only the transmission of these signals, but also their timing and duration. Such timescale regulation is well described for fluctuating chemical signals, but if and how it applies to mechanical signals reaching the nucleus is still unknown. Here we demonstrate that the formation of fibrillar adhesions locks the nucleus in a mechanically deformed conformation, setting the mechanical response timescale to that of fibrillar adhesion remodelling (~1 hour). This process encompasses both mechanical deformation and associated mechanotransduction (such as via YAP), in response to both increased and decreased mechanical stimulation. The underlying mechanism is the anchoring of the vimentin cytoskeleton to fibrillar adhesions and the extracellular matrix through plectin 1f, which maintains nuclear deformation. Our results reveal a mechanism to regulate the timescale of mechanical adaptation, effectively setting a low pass filter to mechanotransduction. Cold Spring Harbor Laboratory 2023-11-11 /pmc/articles/PMC10659263/ /pubmed/37986921 http://dx.doi.org/10.1101/2023.11.08.566191 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Beedle, Amy E.M. Jaganathan, Anuja Albajar-Sigalés, Aina Yavitt, F. Max Bera, Kaustav Andreu, Ion Granero-Moya, Ignasi Zalvidea, Dobryna Kechagia, Zanetta Wiche, Gerhard Trepat, Xavier Ivaska, Johanna Anseth, Kristi S. Shenoy, Vivek B. Roca-Cusachs, Pere Fibrillar adhesion dynamics govern the timescales of nuclear mechano-response via the vimentin cytoskeleton |
title | Fibrillar adhesion dynamics govern the timescales of nuclear mechano-response via the vimentin cytoskeleton |
title_full | Fibrillar adhesion dynamics govern the timescales of nuclear mechano-response via the vimentin cytoskeleton |
title_fullStr | Fibrillar adhesion dynamics govern the timescales of nuclear mechano-response via the vimentin cytoskeleton |
title_full_unstemmed | Fibrillar adhesion dynamics govern the timescales of nuclear mechano-response via the vimentin cytoskeleton |
title_short | Fibrillar adhesion dynamics govern the timescales of nuclear mechano-response via the vimentin cytoskeleton |
title_sort | fibrillar adhesion dynamics govern the timescales of nuclear mechano-response via the vimentin cytoskeleton |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10659263/ https://www.ncbi.nlm.nih.gov/pubmed/37986921 http://dx.doi.org/10.1101/2023.11.08.566191 |
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