Deterministic actin waves as generators of cell polarization cues.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
14 01 2020
Historique:
pubmed: 29 12 2019
medline: 17 4 2020
entrez: 29 12 2019
Statut: ppublish

Résumé

Dendritic cells "patrol" the human body to detect pathogens. In their search, dendritic cells perform a random walk by amoeboid migration. The efficiency of pathogen detection depends on the properties of the random walk. It is not known how the dendritic cells control these properties. Here, we quantify dendritic cell migration under well-defined 2-dimensional confinement and in a 3-dimensional collagen matrix through recording their long-term trajectories. We find 2 different migration states: persistent migration, during which the dendritic cells move along curved paths, and diffusive migration, which is characterized by successive sharp turns. These states exhibit differences in the actin distributions. Our theoretical and experimental analyses indicate that this kind of motion can be generated by spontaneous actin polymerization waves that contribute to dendritic cell polarization and migration. The relative distributions of persistent and diffusive migration can be changed by modification of the molecular actin filament nucleation and assembly rates. Thus, dendritic cells can control their migration patterns and adapt to specific environments. Our study offers an additional perspective on how dendritic cells tune their searches for pathogens.

Identifiants

pubmed: 31882452
pii: 1907845117
doi: 10.1073/pnas.1907845117
pmc: PMC6969493
doi:

Substances chimiques

Actins 0
Gels 0
Collagen 9007-34-5

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

826-835

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Luiza Stankevicins (L)

Bio Interfaces, Leibniz Institute for New Materials, 66123 Saarbrücken, Germany.

Nicolas Ecker (N)

Department of Biochemistry, University of Geneva, 1211 Geneva, Switzerland.
Department of Theoretical Physics, University of Geneva, 1211 Geneva, Switzerland.

Emmanuel Terriac (E)

Bio Interfaces, Leibniz Institute for New Materials, 66123 Saarbrücken, Germany.

Paolo Maiuri (P)

International Foundations of Medicine (IFOM), The Fondazione Italiana per la Ricerca sul Cancro (FIRC) Institute of Molecular Oncology, 20139 Milano, Italy.

Rouven Schoppmeyer (R)

Department of Biophysics, Center for Integrative Physiology and Molecular Medicine, School of Medicine, Saarland University, 66421 Homburg, Germany.

Pablo Vargas (P)

INSERM U932, Institut Curie, 75005 Paris, France.
CNRS UMR144, Institut Curie, 75005 Paris, France.

Ana-Maria Lennon-Duménil (AM)

INSERM U932, Institut Curie, 75005 Paris, France.

Matthieu Piel (M)

Institut Curie, CNRS, UMR 144, Université Paris Sciences et Lettres (PSL) Research University, 75005 Paris, France.
Institut Pierre-Gilles de Gennes, PSL Research University, 75005 Paris, France.

Bin Qu (B)

International Foundations of Medicine (IFOM), The Fondazione Italiana per la Ricerca sul Cancro (FIRC) Institute of Molecular Oncology, 20139 Milano, Italy.

Markus Hoth (M)

Department of Biophysics, Center for Integrative Physiology and Molecular Medicine, School of Medicine, Saarland University, 66421 Homburg, Germany.

Karsten Kruse (K)

Department of Biochemistry, University of Geneva, 1211 Geneva, Switzerland.
Department of Theoretical Physics, University of Geneva, 1211 Geneva, Switzerland.
National Center for Competence in Research Chemical Biology, University of Geneva, 1211 Geneva, Switzerland.

Franziska Lautenschläger (F)

Bio Interfaces, Leibniz Institute for New Materials, 66123 Saarbrücken, Germany; f.lautenschlaeger@physik.uni-saarland.de.
Department of Natural Sciences, Saarland University, 66123 Saarbrücken, Germany.

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