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Mechanics and regulation of cytokinetic abscission

Cytokinetic abscission leads to the physical cut of the intercellular bridge (ICB) connecting the daughter cells and concludes cell division. In different animal cells, it is well established that the ESCRT-III machinery is responsible for the constriction and scission of the ICB. Here, we review th...

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Autores principales: Andrade, Virginia, Echard, Arnaud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730121/
https://www.ncbi.nlm.nih.gov/pubmed/36506096
http://dx.doi.org/10.3389/fcell.2022.1046617
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author Andrade, Virginia
Echard, Arnaud
author_facet Andrade, Virginia
Echard, Arnaud
author_sort Andrade, Virginia
collection PubMed
description Cytokinetic abscission leads to the physical cut of the intercellular bridge (ICB) connecting the daughter cells and concludes cell division. In different animal cells, it is well established that the ESCRT-III machinery is responsible for the constriction and scission of the ICB. Here, we review the mechanical context of abscission. We first summarize the evidence that the ICB is initially under high tension and explain why, paradoxically, this can inhibit abscission in epithelial cells by impacting on ESCRT-III assembly. We next detail the different mechanisms that have been recently identified to release ICB tension and trigger abscission. Finally, we discuss whether traction-induced mechanical cell rupture could represent an ancient alternative mechanism of abscission and suggest future research avenues to further understand the role of mechanics in regulating abscission.
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spelling pubmed-97301212022-12-09 Mechanics and regulation of cytokinetic abscission Andrade, Virginia Echard, Arnaud Front Cell Dev Biol Cell and Developmental Biology Cytokinetic abscission leads to the physical cut of the intercellular bridge (ICB) connecting the daughter cells and concludes cell division. In different animal cells, it is well established that the ESCRT-III machinery is responsible for the constriction and scission of the ICB. Here, we review the mechanical context of abscission. We first summarize the evidence that the ICB is initially under high tension and explain why, paradoxically, this can inhibit abscission in epithelial cells by impacting on ESCRT-III assembly. We next detail the different mechanisms that have been recently identified to release ICB tension and trigger abscission. Finally, we discuss whether traction-induced mechanical cell rupture could represent an ancient alternative mechanism of abscission and suggest future research avenues to further understand the role of mechanics in regulating abscission. Frontiers Media S.A. 2022-11-24 /pmc/articles/PMC9730121/ /pubmed/36506096 http://dx.doi.org/10.3389/fcell.2022.1046617 Text en Copyright © 2022 Andrade and Echard. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Andrade, Virginia
Echard, Arnaud
Mechanics and regulation of cytokinetic abscission
title Mechanics and regulation of cytokinetic abscission
title_full Mechanics and regulation of cytokinetic abscission
title_fullStr Mechanics and regulation of cytokinetic abscission
title_full_unstemmed Mechanics and regulation of cytokinetic abscission
title_short Mechanics and regulation of cytokinetic abscission
title_sort mechanics and regulation of cytokinetic abscission
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730121/
https://www.ncbi.nlm.nih.gov/pubmed/36506096
http://dx.doi.org/10.3389/fcell.2022.1046617
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