Actomyosin-driven force patterning controls endocytosis at the immune synapse.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
28 06 2019
Historique:
received: 27 03 2019
accepted: 30 05 2019
entrez: 30 6 2019
pubmed: 30 6 2019
medline: 28 8 2019
Statut: epublish

Résumé

An important channel of cell-to-cell communication is direct contact. The immune synapse is a paradigmatic example of such type of interaction: it forms upon engagement of antigen receptors in lymphocytes by antigen-presenting cells and allows the local exchange of molecules and information. Although mechanics has been shown to play an important role in this process, how forces organize and impact on synapse function is unknown. We find that mechanical forces are spatio-temporally patterned at the immune synapse: global pulsatile myosin II-driven tangential forces are observed at the synapse periphery while localised forces generated by invadosome-like F-actin protrusions are detected at its centre. Noticeably, we observe that these force-producing actin protrusions constitute the main site of antigen extraction and endocytosis and require myosin II contractility to form. The interplay between global and local forces dictated by the organization of the actomyosin cytoskeleton therefore controls endocytosis at the immune synapse.

Identifiants

pubmed: 31253773
doi: 10.1038/s41467-019-10751-7
pii: 10.1038/s41467-019-10751-7
pmc: PMC6599028
doi:

Substances chimiques

Receptors, Complement 3d 0
Actomyosin 9013-26-7
Cre recombinase EC 2.7.7.-
Integrases EC 2.7.7.-
Myosin Type II EC 3.6.1.-

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2870

Subventions

Organisme : Agence Nationale de la Recherche (French National Research Agency)
ID : ANR-10-JCJC-1504-Immuphy
Pays : International

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Auteurs

Anita Kumari (A)

Institut Curie, PSL Research University, INSERM U932, 26 rue d'Ulm, 75248, Paris, Cedex 05, France.
Université Paris Descartes, Paris, 75006, France.

Judith Pineau (J)

Institut Curie, PSL Research University, INSERM U932, 26 rue d'Ulm, 75248, Paris, Cedex 05, France.
Université Paris Descartes, Paris, 75006, France.

Pablo J Sáez (PJ)

Institut Curie, PSL Research University, INSERM U932, 26 rue d'Ulm, 75248, Paris, Cedex 05, France.

Mathieu Maurin (M)

Institut Curie, PSL Research University, INSERM U932, 26 rue d'Ulm, 75248, Paris, Cedex 05, France.

Danielle Lankar (D)

Institut Curie, PSL Research University, INSERM U932, 26 rue d'Ulm, 75248, Paris, Cedex 05, France.

Mabel San Roman (M)

Institut Curie, PSL Research University, INSERM U932, 26 rue d'Ulm, 75248, Paris, Cedex 05, France.

Katharina Hennig (K)

Laboratoire Interdisciplinaire de Physique, Université Joseph Fourier (Grenoble 1), 38402, Saint, Martin d'Hères Cedex 9, France.

Vanessa F Boura (VF)

Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, 17177, Sweden.

Raphael Voituriez (R)

Laboratoire de Physique Théorique de la Matière Condensée, UMR 7600 CNRS /UPMC and Laboratoire Jean Perrin, UMR 8237 CNRS /UPMC, 4 Place Jussieu, 75255, Paris, Cedex 05, France.

Mikael C I Karlsson (MCI)

Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, 17177, Sweden.

Martial Balland (M)

Laboratoire Interdisciplinaire de Physique, Université Joseph Fourier (Grenoble 1), 38402, Saint, Martin d'Hères Cedex 9, France.

Ana-Maria Lennon Dumenil (AM)

Institut Curie, PSL Research University, INSERM U932, 26 rue d'Ulm, 75248, Paris, Cedex 05, France. ana-maria.lennon@curie.fr.

Paolo Pierobon (P)

Institut Curie, PSL Research University, INSERM U932, 26 rue d'Ulm, 75248, Paris, Cedex 05, France. paolo.pierobon@curie.fr.

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Classifications MeSH