Role of dynamin 2 in the disassembly of focal adhesions

被引:7
作者
Brinas, Laura [1 ,2 ,3 ,4 ]
Vassilopoulos, Stephane [1 ,2 ,3 ,4 ]
Bonne, Gisele [1 ,2 ,3 ,4 ,5 ]
Guicheney, Pascale [6 ]
Bitoun, Marc [1 ,2 ,3 ,4 ]
机构
[1] Univ Paris 06, UM76, F-75013 Paris, France
[2] Univ Paris 06, INSERM, U974, F-75013 Paris, France
[3] CNRS, UMR 7215, Paris, France
[4] Inst Myol, Paris, France
[5] Grp Hosp Pitie Salpetriere, AP HP, UF Cardiogenet & Myogenet, Serv Biochim Metab, F-75013 Paris, France
[6] Univ Paris 06, INSERM, U956, F-75013 Paris, France
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2013年 / 91卷 / 07期
关键词
Dynamin; 2; Focal adhesion; Endocytosis; Focal adhesion disassembly; CALPAIN-MEDIATED PROTEOLYSIS; MARIE-TOOTH DISEASE; ACTIN STRESS FIBERS; INTEGRIN ENDOCYTOSIS; CYTOPLASMIC DOMAIN; CELL-ADHESION; KINASE; PROTEIN; SRC; SYNDECAN-4;
D O I
10.1007/s00109-013-1040-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Dynamin 2 (DNM2) is involved in endocytosis and intracellular membrane trafficking through its function in vesicle formation from distinct membrane compartments. During the last decade, several studies pointed out an important role of DNM2-dependent trafficking in turnover of focal adhesions which represent a physical link between the extracellular matrix and the intracellular actin cytoskeleton, and a platform for several signalling pathways. Here, we review the involvement of DNM2 in structural and functional aspects of the focal adhesion sites. Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy. Potential impairment of focal adhesions as a pathophysiological hypothesis in DNM2-related human diseases is discussed.
引用
收藏
页码:803 / 809
页数:7
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