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Actin dynamics counteract membrane tension during clathrin-mediated endocytosis

Clathrin-mediated endocytosis is independent of actin dynamics in many circumstances but requires actin polymerization in others. We show that membrane tension determines the actin dependence of clathrin-coat assembly. As found previously, clathrin assembly supports formation of mature coated pits i...

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Autores principales: Boulant, Steeve, Kural, Comert, Zeeh, Jean-Christophe, Ubelmann, Florent, Kirchhausen, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3167020/
https://www.ncbi.nlm.nih.gov/pubmed/21841790
http://dx.doi.org/10.1038/ncb2307
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author Boulant, Steeve
Kural, Comert
Zeeh, Jean-Christophe
Ubelmann, Florent
Kirchhausen, Tom
author_facet Boulant, Steeve
Kural, Comert
Zeeh, Jean-Christophe
Ubelmann, Florent
Kirchhausen, Tom
author_sort Boulant, Steeve
collection PubMed
description Clathrin-mediated endocytosis is independent of actin dynamics in many circumstances but requires actin polymerization in others. We show that membrane tension determines the actin dependence of clathrin-coat assembly. As found previously, clathrin assembly supports formation of mature coated pits in the absence of actin polymerization on both dorsal and ventral surfaces of non-polarized mammalian cells, and also on basolateral surfaces of polarized cells. Actin engagement is necessary, however, to complete membrane deformation into a coated pit on apical surfaces of polarized cells and, more generally, on the surface of any cell in which the plasma membrane is under tension from osmotic swelling or mechanical stretching. We use these observations to alter actin dependence experimentally and show that resistance of the membrane to propagation of the clathrin lattice determines the distinction between "actin-dependent" and "actin-independent". We also find that light-chain bound Hip1R mediates actin engagement. These data thus provide a unifying explanation for the role of actin dynamics in coated-pit budding.
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spelling pubmed-31670202012-03-01 Actin dynamics counteract membrane tension during clathrin-mediated endocytosis Boulant, Steeve Kural, Comert Zeeh, Jean-Christophe Ubelmann, Florent Kirchhausen, Tom Nat Cell Biol Article Clathrin-mediated endocytosis is independent of actin dynamics in many circumstances but requires actin polymerization in others. We show that membrane tension determines the actin dependence of clathrin-coat assembly. As found previously, clathrin assembly supports formation of mature coated pits in the absence of actin polymerization on both dorsal and ventral surfaces of non-polarized mammalian cells, and also on basolateral surfaces of polarized cells. Actin engagement is necessary, however, to complete membrane deformation into a coated pit on apical surfaces of polarized cells and, more generally, on the surface of any cell in which the plasma membrane is under tension from osmotic swelling or mechanical stretching. We use these observations to alter actin dependence experimentally and show that resistance of the membrane to propagation of the clathrin lattice determines the distinction between "actin-dependent" and "actin-independent". We also find that light-chain bound Hip1R mediates actin engagement. These data thus provide a unifying explanation for the role of actin dynamics in coated-pit budding. 2011-08-14 /pmc/articles/PMC3167020/ /pubmed/21841790 http://dx.doi.org/10.1038/ncb2307 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Boulant, Steeve
Kural, Comert
Zeeh, Jean-Christophe
Ubelmann, Florent
Kirchhausen, Tom
Actin dynamics counteract membrane tension during clathrin-mediated endocytosis
title Actin dynamics counteract membrane tension during clathrin-mediated endocytosis
title_full Actin dynamics counteract membrane tension during clathrin-mediated endocytosis
title_fullStr Actin dynamics counteract membrane tension during clathrin-mediated endocytosis
title_full_unstemmed Actin dynamics counteract membrane tension during clathrin-mediated endocytosis
title_short Actin dynamics counteract membrane tension during clathrin-mediated endocytosis
title_sort actin dynamics counteract membrane tension during clathrin-mediated endocytosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3167020/
https://www.ncbi.nlm.nih.gov/pubmed/21841790
http://dx.doi.org/10.1038/ncb2307
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