Annexin-A5 assembled into two-dimensional arrays promotes cell membrane repair

Anthony Bouter, Céline Gounou(Institut National Polytechnique de Toulouse), Rémi Bérat(Institut Européen de Chimie et Biologie), Sisareuth Tan(Institut Européen de Chimie et Biologie), B. Gallois(Laboratoire des Biomolécules), T. Granier(Laboratoire des Biomolécules), Béatrice Langlois d’Estaintot(Laboratoire des Biomolécules), Ernst Pöschl(University of East Anglia), Bent Brachvogel(University of Cologne), Alain Brisson(Institut Européen de Chimie et Biologie)
Nature Communications
April 5, 2011
Cited by 278Open Access
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Abstract

Eukaryotic cells possess a universal repair machinery that ensures rapid resealing of plasma membrane disruptions. Before resealing, the torn membrane is submitted to considerable tension, which functions to expand the disruption. Here we show that annexin-A5 (AnxA5), a protein that self-assembles into two-dimensional (2D) arrays on membranes upon Ca2+ activation, promotes membrane repair. Compared with wild-type mouse perivascular cells, AnxA5-null cells exhibit a severe membrane repair defect. Membrane repair in AnxA5-null cells is rescued by addition of AnxA5, which binds exclusively to disrupted membrane areas. In contrast, an AnxA5 mutant that lacks the ability of forming 2D arrays is unable to promote membrane repair. We propose that AnxA5 participates in a previously unrecognized step of the membrane repair process: triggered by the local influx of Ca2+, AnxA5 proteins bind to torn membrane edges and form a 2D array, which prevents wound expansion and promotes membrane resealing. Eukaryotic cell plasma membranes possess a mechanism to repair tears caused by stimuli such as mechanical stress. The authors demonstrate that annexin-A5, when assembled into two-dimensional arrays in the presence of calcium, is required for membrane repair.


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