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Caveolin-1 dolines form a distinct and rapid caveolae-independent mechanoadaptation system
In response to different types and intensities of mechanical force, cells modulate their physical properties and adapt their plasma membrane (PM). Caveolae are PM nano-invaginations that contribute to mechanoadaptation, buffering tension changes. However, whether core caveolar proteins contribute to...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859760/ https://www.ncbi.nlm.nih.gov/pubmed/36543981 http://dx.doi.org/10.1038/s41556-022-01034-3 |
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author | Lolo, Fidel-Nicolás Walani, Nikhil Seemann, Eric Zalvidea, Dobryna Pavón, Dácil María Cojoc, Gheorghe Zamai, Moreno Viaris de Lesegno, Christine Martínez de Benito, Fernando Sánchez-Álvarez, Miguel Uriarte, Juan José Echarri, Asier Jiménez-Carretero, Daniel Escolano, Joan-Carles Sánchez, Susana A. Caiolfa, Valeria R. Navajas, Daniel Trepat, Xavier Guck, Jochen Lamaze, Christophe Roca-Cusachs, Pere Kessels, Michael M. Qualmann, Britta Arroyo, Marino del Pozo, Miguel A. |
author_facet | Lolo, Fidel-Nicolás Walani, Nikhil Seemann, Eric Zalvidea, Dobryna Pavón, Dácil María Cojoc, Gheorghe Zamai, Moreno Viaris de Lesegno, Christine Martínez de Benito, Fernando Sánchez-Álvarez, Miguel Uriarte, Juan José Echarri, Asier Jiménez-Carretero, Daniel Escolano, Joan-Carles Sánchez, Susana A. Caiolfa, Valeria R. Navajas, Daniel Trepat, Xavier Guck, Jochen Lamaze, Christophe Roca-Cusachs, Pere Kessels, Michael M. Qualmann, Britta Arroyo, Marino del Pozo, Miguel A. |
author_sort | Lolo, Fidel-Nicolás |
collection | PubMed |
description | In response to different types and intensities of mechanical force, cells modulate their physical properties and adapt their plasma membrane (PM). Caveolae are PM nano-invaginations that contribute to mechanoadaptation, buffering tension changes. However, whether core caveolar proteins contribute to PM tension accommodation independently from the caveolar assembly is unknown. Here we provide experimental and computational evidence supporting that caveolin-1 confers deformability and mechanoprotection independently from caveolae, through modulation of PM curvature. Freeze-fracture electron microscopy reveals that caveolin-1 stabilizes non-caveolar invaginations—dolines—capable of responding to low-medium mechanical forces, impacting downstream mechanotransduction and conferring mechanoprotection to cells devoid of caveolae. Upon cavin-1/PTRF binding, doline size is restricted and membrane buffering is limited to relatively high forces, capable of flattening caveolae. Thus, caveolae and dolines constitute two distinct albeit complementary components of a buffering system that allows cells to adapt efficiently to a broad range of mechanical stimuli. |
format | Online Article Text |
id | pubmed-9859760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98597602023-01-22 Caveolin-1 dolines form a distinct and rapid caveolae-independent mechanoadaptation system Lolo, Fidel-Nicolás Walani, Nikhil Seemann, Eric Zalvidea, Dobryna Pavón, Dácil María Cojoc, Gheorghe Zamai, Moreno Viaris de Lesegno, Christine Martínez de Benito, Fernando Sánchez-Álvarez, Miguel Uriarte, Juan José Echarri, Asier Jiménez-Carretero, Daniel Escolano, Joan-Carles Sánchez, Susana A. Caiolfa, Valeria R. Navajas, Daniel Trepat, Xavier Guck, Jochen Lamaze, Christophe Roca-Cusachs, Pere Kessels, Michael M. Qualmann, Britta Arroyo, Marino del Pozo, Miguel A. Nat Cell Biol Article In response to different types and intensities of mechanical force, cells modulate their physical properties and adapt their plasma membrane (PM). Caveolae are PM nano-invaginations that contribute to mechanoadaptation, buffering tension changes. However, whether core caveolar proteins contribute to PM tension accommodation independently from the caveolar assembly is unknown. Here we provide experimental and computational evidence supporting that caveolin-1 confers deformability and mechanoprotection independently from caveolae, through modulation of PM curvature. Freeze-fracture electron microscopy reveals that caveolin-1 stabilizes non-caveolar invaginations—dolines—capable of responding to low-medium mechanical forces, impacting downstream mechanotransduction and conferring mechanoprotection to cells devoid of caveolae. Upon cavin-1/PTRF binding, doline size is restricted and membrane buffering is limited to relatively high forces, capable of flattening caveolae. Thus, caveolae and dolines constitute two distinct albeit complementary components of a buffering system that allows cells to adapt efficiently to a broad range of mechanical stimuli. Nature Publishing Group UK 2022-12-21 2023 /pmc/articles/PMC9859760/ /pubmed/36543981 http://dx.doi.org/10.1038/s41556-022-01034-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lolo, Fidel-Nicolás Walani, Nikhil Seemann, Eric Zalvidea, Dobryna Pavón, Dácil María Cojoc, Gheorghe Zamai, Moreno Viaris de Lesegno, Christine Martínez de Benito, Fernando Sánchez-Álvarez, Miguel Uriarte, Juan José Echarri, Asier Jiménez-Carretero, Daniel Escolano, Joan-Carles Sánchez, Susana A. Caiolfa, Valeria R. Navajas, Daniel Trepat, Xavier Guck, Jochen Lamaze, Christophe Roca-Cusachs, Pere Kessels, Michael M. Qualmann, Britta Arroyo, Marino del Pozo, Miguel A. Caveolin-1 dolines form a distinct and rapid caveolae-independent mechanoadaptation system |
title | Caveolin-1 dolines form a distinct and rapid caveolae-independent mechanoadaptation system |
title_full | Caveolin-1 dolines form a distinct and rapid caveolae-independent mechanoadaptation system |
title_fullStr | Caveolin-1 dolines form a distinct and rapid caveolae-independent mechanoadaptation system |
title_full_unstemmed | Caveolin-1 dolines form a distinct and rapid caveolae-independent mechanoadaptation system |
title_short | Caveolin-1 dolines form a distinct and rapid caveolae-independent mechanoadaptation system |
title_sort | caveolin-1 dolines form a distinct and rapid caveolae-independent mechanoadaptation system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859760/ https://www.ncbi.nlm.nih.gov/pubmed/36543981 http://dx.doi.org/10.1038/s41556-022-01034-3 |
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