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EHD2 is a mechanotransducer connecting caveolae dynamics with gene transcription
Caveolae are small invaginated pits that function as dynamic mechanosensors to buffer tension variations at the plasma membrane. Here we show that under mechanical stress, the EHD2 ATPase is rapidly released from caveolae, SUMOylated, and translocated to the nucleus, where it regulates the transcrip...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279385/ https://www.ncbi.nlm.nih.gov/pubmed/30348749 http://dx.doi.org/10.1083/jcb.201801122 |
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author | Torrino, Stéphanie Shen, Wei-Wei Blouin, Cédric M. Mani, Satish Kailasam Viaris de Lesegno, Christine Bost, Pierre Grassart, Alexandre Köster, Darius Valades-Cruz, Cesar Augusto Chambon, Valérie Johannes, Ludger Pierobon, Paolo Soumelis, Vassili Coirault, Catherine Vassilopoulos, Stéphane Lamaze, Christophe |
author_facet | Torrino, Stéphanie Shen, Wei-Wei Blouin, Cédric M. Mani, Satish Kailasam Viaris de Lesegno, Christine Bost, Pierre Grassart, Alexandre Köster, Darius Valades-Cruz, Cesar Augusto Chambon, Valérie Johannes, Ludger Pierobon, Paolo Soumelis, Vassili Coirault, Catherine Vassilopoulos, Stéphane Lamaze, Christophe |
author_sort | Torrino, Stéphanie |
collection | PubMed |
description | Caveolae are small invaginated pits that function as dynamic mechanosensors to buffer tension variations at the plasma membrane. Here we show that under mechanical stress, the EHD2 ATPase is rapidly released from caveolae, SUMOylated, and translocated to the nucleus, where it regulates the transcription of several genes including those coding for caveolae constituents. We also found that EHD2 is required to maintain the caveolae reservoir at the plasma membrane during the variations of membrane tension induced by mechanical stress. Metal-replica electron microscopy of breast cancer cells lacking EHD2 revealed a complete absence of caveolae and a lack of gene regulation under mechanical stress. Expressing EHD2 was sufficient to restore both functions in these cells. Our findings therefore define EHD2 as a central player in mechanotransduction connecting the disassembly of the caveolae reservoir with the regulation of gene transcription under mechanical stress. |
format | Online Article Text |
id | pubmed-6279385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62793852019-06-03 EHD2 is a mechanotransducer connecting caveolae dynamics with gene transcription Torrino, Stéphanie Shen, Wei-Wei Blouin, Cédric M. Mani, Satish Kailasam Viaris de Lesegno, Christine Bost, Pierre Grassart, Alexandre Köster, Darius Valades-Cruz, Cesar Augusto Chambon, Valérie Johannes, Ludger Pierobon, Paolo Soumelis, Vassili Coirault, Catherine Vassilopoulos, Stéphane Lamaze, Christophe J Cell Biol Research Articles Caveolae are small invaginated pits that function as dynamic mechanosensors to buffer tension variations at the plasma membrane. Here we show that under mechanical stress, the EHD2 ATPase is rapidly released from caveolae, SUMOylated, and translocated to the nucleus, where it regulates the transcription of several genes including those coding for caveolae constituents. We also found that EHD2 is required to maintain the caveolae reservoir at the plasma membrane during the variations of membrane tension induced by mechanical stress. Metal-replica electron microscopy of breast cancer cells lacking EHD2 revealed a complete absence of caveolae and a lack of gene regulation under mechanical stress. Expressing EHD2 was sufficient to restore both functions in these cells. Our findings therefore define EHD2 as a central player in mechanotransduction connecting the disassembly of the caveolae reservoir with the regulation of gene transcription under mechanical stress. Rockefeller University Press 2018-12-03 /pmc/articles/PMC6279385/ /pubmed/30348749 http://dx.doi.org/10.1083/jcb.201801122 Text en © 2018 Torrino et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Torrino, Stéphanie Shen, Wei-Wei Blouin, Cédric M. Mani, Satish Kailasam Viaris de Lesegno, Christine Bost, Pierre Grassart, Alexandre Köster, Darius Valades-Cruz, Cesar Augusto Chambon, Valérie Johannes, Ludger Pierobon, Paolo Soumelis, Vassili Coirault, Catherine Vassilopoulos, Stéphane Lamaze, Christophe EHD2 is a mechanotransducer connecting caveolae dynamics with gene transcription |
title | EHD2 is a mechanotransducer connecting caveolae dynamics with gene transcription |
title_full | EHD2 is a mechanotransducer connecting caveolae dynamics with gene transcription |
title_fullStr | EHD2 is a mechanotransducer connecting caveolae dynamics with gene transcription |
title_full_unstemmed | EHD2 is a mechanotransducer connecting caveolae dynamics with gene transcription |
title_short | EHD2 is a mechanotransducer connecting caveolae dynamics with gene transcription |
title_sort | ehd2 is a mechanotransducer connecting caveolae dynamics with gene transcription |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279385/ https://www.ncbi.nlm.nih.gov/pubmed/30348749 http://dx.doi.org/10.1083/jcb.201801122 |
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