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An Arf6- and caveolae-dependent pathway links hemidesmosome remodeling and mechanoresponse.

Authors :
Osmani N
Pontabry J
Comelles J
Fekonja N
Goetz JG
Riveline D
Georges-Labouesse E
Labouesse M
Source :
Molecular biology of the cell [Mol Biol Cell] 2018 Feb 15; Vol. 29 (4), pp. 435-451. Date of Electronic Publication: 2017 Dec 13.
Publication Year :
2018

Abstract

Hemidesmosomes (HDs) are epithelial-specific cell-matrix adhesions that stably anchor the intracellular keratin network to the extracellular matrix. Although their main role is to protect the epithelial sheet from external mechanical strain, how HDs respond to mechanical stress remains poorly understood. Here we identify a pathway essential for HD remodeling and outline its role with respect to α6β4 integrin recycling. We find that α6β4 integrin chains localize to the plasma membrane, caveolae, and ADP-ribosylation factor-6+ (Arf6+) endocytic compartments. Based on fluorescence recovery after photobleaching and endocytosis assays, integrin recycling between both sites requires the small GTPase Arf6 but neither caveolin1 (Cav1) nor Cavin1. Strikingly, when keratinocytes are stretched or hypo-osmotically shocked, α6β4 integrin accumulates at cell edges, whereas Cav1 disappears from it. This process, which is isotropic relative to the orientation of stretch, depends on Arf6, Cav1, and Cavin1. We propose that mechanically induced HD growth involves the isotropic flattening of caveolae (known for their mechanical buffering role) associated with integrin diffusion and turnover.<br /> (© 2018 Osmani et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).)

Details

Language :
English
ISSN :
1939-4586
Volume :
29
Issue :
4
Database :
MEDLINE
Journal :
Molecular biology of the cell
Publication Type :
Academic Journal
Accession number :
29237817
Full Text :
https://doi.org/10.1091/mbc.E17-06-0356