Actin modulates shape and mechanics of tubular membranes.


Journal

Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440

Informations de publication

Date de publication:
04 2020
Historique:
received: 28 08 2019
accepted: 21 01 2020
entrez: 5 6 2020
pubmed: 5 6 2020
medline: 5 6 2020
Statut: epublish

Résumé

The actin cytoskeleton shapes cells and also organizes internal membranous compartments. In particular, it interacts with membranes for intracellular transport of material in mammalian cells, yeast, or plant cells. Tubular membrane intermediates, pulled along microtubule tracks, are formed during this process and destabilize into vesicles. While the role of actin in tubule destabilization through scission is suggested, literature also provides examples of actin-mediated stabilization of membranous structures. To directly address this apparent contradiction, we mimic the geometry of tubular intermediates with preformed membrane tubes. The growth of an actin sleeve at the tube surface is monitored spatiotemporally. Depending on network cohesiveness, actin is able to entirely stabilize or locally maintain membrane tubes under pulling. On a single tube, thicker portions correlate with the presence of actin. These structures relax over several minutes and may provide enough time and curvature geometries for other proteins to act on tube stability.

Identifiants

pubmed: 32494637
doi: 10.1126/sciadv.aaz3050
pii: aaz3050
pmc: PMC7176416
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

eaaz3050

Informations de copyright

Copyright © 2020 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).

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Auteurs

A Allard (A)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.
LAMBE, Université Évry Val d'Essonne, CNRS, CEA, Université Paris-Saclay, Évry, France.

M Bouzid (M)

LPTMS, CNRS, University of Paris-Sud, Universit Paris-Saclay, 91405 Orsay, France.

T Betz (T)

Institute of Cell Biology, Center for Molecular Biology of Inflammation, Cells in Motion Cluster of Excellence, Münster University, Von-Esmarch-Strasse 56, D-48149 Münster, Germany.

C Simon (C)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.

M Abou-Ghali (M)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.

J Lemière (J)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.

F Valentino (F)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.

J Manzi (J)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.

F Brochard-Wyart (F)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.

K Guevorkian (K)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.

J Plastino (J)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.

M Lenz (M)

LPTMS, CNRS, University of Paris-Sud, Universit Paris-Saclay, 91405 Orsay, France.
Laboratoire de Physique et Mécanique des Milieux Hétérogènes, UMR 7636, CNRS, ESPCI Paris, PSL Research University, Université Paris Diderot, Sorbonne Université, Paris 75005, France.

C Campillo (C)

LAMBE, Université Évry Val d'Essonne, CNRS, CEA, Université Paris-Saclay, Évry, France.

C Sykes (C)

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.

Classifications MeSH