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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...

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Autores principales: Andrade, Virginia, Bai, Jian, Gupta-Rossi, Neetu, Jimenez, Ana Joaquina, Delevoye, Cédric, Lamaze, Christophe, Echard, Arnaud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
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.
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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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