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Mechanism of Ca²⁺-triggered ESCRT assembly and regulation of cell membrane repair.
- Source :
-
Nature communications [Nat Commun] 2014 Dec 23; Vol. 5, pp. 5646. Date of Electronic Publication: 2014 Dec 23. - Publication Year :
- 2014
-
Abstract
- In muscle and other mechanically active tissue, cell membranes are constantly injured, and their repair depends on the injury-induced increase in cytosolic calcium. Here, we show that injury-triggered Ca(2+) increase results in assembly of ESCRT III and accessory proteins at the site of repair. This process is initiated by the calcium-binding protein-apoptosis-linked gene (ALG)-2. ALG-2 facilitates accumulation of ALG-2-interacting protein X (ALIX), ESCRT III and Vps4 complex at the injured cell membrane, which in turn results in cleavage and shedding of the damaged part of the cell membrane. Lack of ALG-2, ALIX or Vps4B each prevents shedding, and repair of the injured cell membrane. These results demonstrate Ca(2+)-dependent accumulation of ESCRT III-Vps4 complex following large focal injury to the cell membrane and identify the role of ALG-2 as the initiator of sequential ESCRT III-Vps4 complex assembly that facilitates scission and repair of the injured cell membrane.
- Subjects :
- ATPases Associated with Diverse Cellular Activities
Adenosine Triphosphatases genetics
Animals
Apoptosis Regulatory Proteins genetics
Calcium-Binding Proteins genetics
Cell Cycle Proteins genetics
Cell Membrane enzymology
Cell Membrane genetics
Endosomal Sorting Complexes Required for Transport genetics
Humans
Mice
Myoblasts enzymology
Myoblasts metabolism
Protein Multimerization
Vacuolar Proton-Translocating ATPases genetics
Adenosine Triphosphatases metabolism
Apoptosis Regulatory Proteins metabolism
Calcium metabolism
Calcium-Binding Proteins metabolism
Cell Cycle Proteins metabolism
Cell Membrane metabolism
Endosomal Sorting Complexes Required for Transport metabolism
Vacuolar Proton-Translocating ATPases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 5
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 25534348
- Full Text :
- https://doi.org/10.1038/ncomms6646