Annexin A2 Mediates Dysferlin Accumulation and Muscle Cell Membrane Repair

被引:41
作者
Bittel, Daniel C. [1 ]
Chandra, Goutam [1 ]
Tirunagri, Laxmi M. S. [2 ]
Deora, Arun B. [3 ]
Medikayala, Sushma [1 ]
Scheffer, Luana [1 ]
Defour, Aurelia [1 ]
Jaiswal, Jyoti K. [1 ,4 ]
机构
[1] Natl Childrens Hosp, Ctr Genet Med Res, 111 Michigan Av NW, Washington, DC 20010 USA
[2] Rockefeller Univ, Dept Cellular Biophys, New York, NY 10065 USA
[3] Weill Cornell Med Coll, Dept Cell & Dev Biol, New York, NY 10065 USA
[4] George Washington Univ, Sch Med & Hlth Sci, Dept Genom & Precis Med, Washington, DC 20010 USA
关键词
muscle injury; plasma membrane; vesicle; muscular dystrophy; MUSCULAR-DYSTROPHY; VESICLE FUSION; EXOCYTOSIS; PROTEIN; DISRUPTION; CAVEOLIN-3; DAMAGE; MG53;
D O I
10.3390/cells9091919
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Muscle cell plasma membrane is frequently damaged by mechanical activity, and its repair requires the membrane protein dysferlin. We previously identified that, similar to dysferlin deficit, lack of annexin A2 (AnxA2) also impairs repair of skeletal myofibers. Here, we have studied the mechanism of AnxA2-mediated muscle cell membrane repair in cultured muscle cells. We find that injury-triggered increase in cytosolic calcium causes AnxA2 to bind dysferlin and accumulate on dysferlin-containing vesicles as well as with dysferlin at the site of membrane injury. AnxA2 accumulates on the injured plasma membrane in cholesterol-rich lipid microdomains and requires Src kinase activity and the presence of cholesterol. Lack of AnxA2 and its failure to translocate to the plasma membrane, both prevent calcium-triggered dysferlin translocation to the plasma membrane and compromise repair of the injured plasma membrane. Our studies identify that Anx2 senses calcium increase and injury-triggered change in plasma membrane cholesterol to facilitate dysferlin delivery and repair of the injured plasma membrane.
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页数:17
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