The ALS- and FTD-associated proteins annexin A11 and CHMP2B act sequentially in plasma membrane repair

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Authors: Catherine M Heffner, Georgina P. Starling, Lorian Cobra Straker, Philippa C. Hawes, Adrian M. Isaacs, Jeremy Graham Carlton
Cited by: 1
References: 87

Abstract

Maintenance of plasma membrane integrity is essential for compartmentalization of the cytosol and for cellular viability. Upon membrane damage, several factors including endosomal sorting complex required for transport-III (ESCRT-III) proteins, annexins, stress granules, lipids, and membrane fusion proteins are mobilized to orchestrate membrane repair. However, whether these factors operate independently or act together is unclear. Here, using human cell lines, we expose temporal differences and interdependencies in the recruitment of ESCRT-III and annexin proteins to sites of plasma membrane damage. We show that annexin proteins are recruited immediately and form a plug at the damage site, restricting membrane permeability. We find that ESCRT-III assembles later and acts to release plug-containing damaged membranes from the cell. Further, frontotemporal dementia (FTD)- and amyotrophic lateral sclerosis (ALS)-associated mutations in the ESCRT-III protein, CHMP2B, and the annexin protein, ANXA11, compromise plasma membrane repair, suggesting that defects in this process may contribute to these pathologies. These data present an integrated "sealing and healing" model of membrane repair.

Fields of Study & Subjects

S100 Proteins and Annexins Cellular transport and secretion Amyotrophic Lateral Sclerosis Research

Publication details

Journal / source
Developmental Cell
Publisher
Elsevier BV
Volume
61
Issue
7
Pages
1487–1503.e7
Publication date
25 June 2026
Language
EN