Abstract

Ca2+ entering a cell through a torn or disrupted plasma membrane rapidly triggers a combination of homotypic and exocytotic membrane fusion events. These events serve to erect a reparative membrane patch and then anneal it to the defect site. Annexin A1 is a cytosolic protein that, when activated by micromolar Ca2+, binds to membrane phospholipids, promoting membrane aggregation and fusion. We demonstrate here that an annexin A1 function-blocking antibody, a small peptide competitor, and a dominant-negative annexin A1 mutant protein incapable of Ca2+ binding all inhibit resealing. Moreover, we show that, coincident with a resealing event, annexin A1 becomes concentrated at disruption sites. We propose that Ca2+ entering through a disruption locally induces annexin A1 binding to membranes, initiating emergency fusion events whenever and wherever required.

Highlights

  • The mechanism of resealing is well characterized at the cellular level

  • One protein shown by immunolocalization and immunoprecipitation to associate with dysferlin in normal, undisturbed skeletal muscle is annexin A1 (11), a member of the annexin family of Ca2ϩ-regulated membrane-binding proteins (12)

  • Humans with Duchenne muscular dystrophy, in which the frequency of sacrolemma disruption is greatly increased, exhibit enhanced levels of skeletal muscle annexin expression (13), and humans with dysferlin-related muscular dystrophy exhibit an increase in annexin A1 expression (14)

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Summary

Introduction

The mechanism of resealing is well characterized at the cellular level. A large plasma membrane disruption (Ͼ1 ␮m diameter) locally and rapidly (subsecond to second time scale) elicits Ca2ϩ-activated, homotypic vesicle fusion (4, 5). It suggested that the antibody might have an effect on repair of the disruption through which it was entering and that the most heavily wounded cells in the population were failing to reseal and to trap the FDx. To test this possibility quantitatively, cells were scraped in saline containing anti-annexin A1 antibody and FDx or containing FDx only, and the populations analyzed immediately by FACS.

Results
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