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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
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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. |
format | Online Article Text |
id | pubmed-3167020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
record_format | MEDLINE/PubMed |
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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