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Caveolae promote successful abscission by controlling intercellular bridge tension during cytokinesis
During cytokinesis, the intercellular bridge (ICB) connecting the daughter cells experiences pulling forces, which delay abscission by preventing the assembly of the ESCRT scission machinery. Abscission is thus triggered by tension release, but how ICB tension is controlled is unknown. Here, we repo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007517/ https://www.ncbi.nlm.nih.gov/pubmed/35417244 http://dx.doi.org/10.1126/sciadv.abm5095 |
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author | Andrade, Virginia Bai, Jian Gupta-Rossi, Neetu Jimenez, Ana Joaquina Delevoye, Cédric Lamaze, Christophe Echard, Arnaud |
author_facet | Andrade, Virginia Bai, Jian Gupta-Rossi, Neetu Jimenez, Ana Joaquina Delevoye, Cédric Lamaze, Christophe Echard, Arnaud |
author_sort | Andrade, Virginia |
collection | PubMed |
description | During cytokinesis, the intercellular bridge (ICB) connecting the daughter cells experiences pulling forces, which delay abscission by preventing the assembly of the ESCRT scission machinery. Abscission is thus triggered by tension release, but how ICB tension is controlled is unknown. Here, we report that caveolae, which are known to regulate membrane tension upon mechanical stress in interphase cells, are located at the midbody, at the abscission site, and at the ICB/cell interface in dividing cells. Functionally, the loss of caveolae delays ESCRT-III recruitment during cytokinesis and impairs abscission. This is the consequence of a twofold increase of ICB tension measured by laser ablation, associated with a local increase in myosin II activity at the ICB/cell interface. We thus propose that caveolae buffer membrane tension and limit contractibility at the ICB to promote ESCRT-III assembly and cytokinetic abscission. Together, this work reveals an unexpected connection between caveolae and the ESCRT machinery and the first role of caveolae in cell division. |
format | Online Article Text |
id | pubmed-9007517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90075172022-04-22 Caveolae promote successful abscission by controlling intercellular bridge tension during cytokinesis Andrade, Virginia Bai, Jian Gupta-Rossi, Neetu Jimenez, Ana Joaquina Delevoye, Cédric Lamaze, Christophe Echard, Arnaud Sci Adv Biomedicine and Life Sciences During cytokinesis, the intercellular bridge (ICB) connecting the daughter cells experiences pulling forces, which delay abscission by preventing the assembly of the ESCRT scission machinery. Abscission is thus triggered by tension release, but how ICB tension is controlled is unknown. Here, we report that caveolae, which are known to regulate membrane tension upon mechanical stress in interphase cells, are located at the midbody, at the abscission site, and at the ICB/cell interface in dividing cells. Functionally, the loss of caveolae delays ESCRT-III recruitment during cytokinesis and impairs abscission. This is the consequence of a twofold increase of ICB tension measured by laser ablation, associated with a local increase in myosin II activity at the ICB/cell interface. We thus propose that caveolae buffer membrane tension and limit contractibility at the ICB to promote ESCRT-III assembly and cytokinetic abscission. Together, this work reveals an unexpected connection between caveolae and the ESCRT machinery and the first role of caveolae in cell division. American Association for the Advancement of Science 2022-04-13 /pmc/articles/PMC9007517/ /pubmed/35417244 http://dx.doi.org/10.1126/sciadv.abm5095 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Andrade, Virginia Bai, Jian Gupta-Rossi, Neetu Jimenez, Ana Joaquina Delevoye, Cédric Lamaze, Christophe Echard, Arnaud Caveolae promote successful abscission by controlling intercellular bridge tension during cytokinesis |
title | Caveolae promote successful abscission by controlling intercellular bridge tension during cytokinesis |
title_full | Caveolae promote successful abscission by controlling intercellular bridge tension during cytokinesis |
title_fullStr | Caveolae promote successful abscission by controlling intercellular bridge tension during cytokinesis |
title_full_unstemmed | Caveolae promote successful abscission by controlling intercellular bridge tension during cytokinesis |
title_short | Caveolae promote successful abscission by controlling intercellular bridge tension during cytokinesis |
title_sort | caveolae promote successful abscission by controlling intercellular bridge tension during cytokinesis |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007517/ https://www.ncbi.nlm.nih.gov/pubmed/35417244 http://dx.doi.org/10.1126/sciadv.abm5095 |
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