Actin dynamics switches two distinct modes of endosomal fusion in yolk sac visceral endoderm cells.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
23 Oct 2024
Historique:
medline: 23 10 2024
pubmed: 23 10 2024
entrez: 23 10 2024
Statut: epublish

Résumé

Membranes undergo various patterns of deformation during vesicle fusion, but how this membrane deformation is regulated and contributes to fusion remains unknown. In this study, we developed a new method of observing the fusion of individual late endosomes and lysosomes by using mouse yolk sac visceral endoderm cells that have huge endocytic vesicles. We found that there were two distinct fusion modes that were differently regulated. In homotypic fusion, two late endosomes fused quickly, whereas in heterotypic fusion they fused to lysosomes slowly. Mathematical modeling showed that vesicle size is a critical determinant of these fusion types and that membrane fluctuation forces can overcome the vesicle size effects. We found that actin filaments were bound to late endosomes and forces derived from dynamic actin remodeling were necessary for quick fusion during homotypic fusion. Furthermore, cofilin played a role in endocytic fusion by regulating actin turnover. These data suggest that actin promotes vesicle fusion for efficient membrane trafficking in visceral endoderm cells.

Identifiants

pubmed: 39441732
doi: 10.7554/eLife.95999
pii: 95999
doi:
pii:

Substances chimiques

Actins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Ministry of Education, Culture, Sports, Science and Technology
ID : KAKENHI (17024006)
Organisme : Japan Society for the Promotion of Science
ID : KAKENHI (JP22H04926)
Organisme : Takeda Science Foundation
ID : 2022039209

Informations de copyright

© 2024, Koike et al.

Déclaration de conflit d'intérêts

SK, MT, MT, TO, TN, KK, MM No competing interests declared

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Auteurs

Seiichi Koike (S)

Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.
Department of Molecular Neurobiology, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.
Laboratory of Molecular and Cellular Biology, Graduate School of Science and Engineering for Research, University of Toyama, Toyama, Japan.

Masashi Tachikawa (M)

Graduate School of Nanobioscience, Yokohama City University, Yokohama, Japan.

Motosuke Tsutsumi (M)

Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences, Okazaki, Japan.
National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Japan.

Takuya Okada (T)

Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.
Department of Molecular Neurobiology, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.

Tomomi Nemoto (T)

Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences, Okazaki, Japan.
National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Japan.

Kazuko Keino-Masu (K)

Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.
Department of Molecular Neurobiology, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.

Masayuki Masu (M)

Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.
Department of Molecular Neurobiology, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.

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