M-cadherin activates Rac1 GTPase through the Rho-GEF trio during myoblast fusion

被引:111
作者
Charrasse, Sophie [1 ]
Comunale, Franck [1 ]
Fortier, Mathieu [1 ]
Portales-Casamar, Elodie [1 ]
Debant, Anne [1 ]
Gauthier-Rouviere, Cecile [1 ]
机构
[1] CNRS, Ctr Rech Biochim Macromol, IFR 122, F-34293 Montpellier, France
关键词
D O I
10.1091/mbc.E06-08-0766
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cadherins are transmembrane glycoproteins that mediate Call-dependent homophilic cell-cell adhesion and play crucial role during skeletal myogenesis. M-cadherin is required for myoblast fusion into myotubes, but its mechanisms of action remain unknown. The goal of this study was to cast some light on the nature of the M-cadherin-mediated signals involved in myoblast fusion into myotubes. We found that the Rac1 GTPase activity is increased at the time of myoblast fusion and it is required for this process. Moreover, we showed that M-cadherin-dependent adhesion activates Rac1 and demonstrated the formation of a multiproteic complex containing M-cadherin, the Rho-GEF Trio, and Rac1 at the onset of myoblast fusion. Interestingly, Trio knockdown efficiently blocked both the increase in Rac1-GTP levels, observed after M-cadherin-dependent contact formation, and myoblast fusion. We conclude that M-cadherin-dependent adhesion can activate Rac1 via the Rho-GEF Trio at the time of myoblast fusion.
引用
收藏
页码:1734 / 1743
页数:10
相关论文
共 61 条
[31]   M-cadherin-mediated cell adhesion and complex formation with the catenins in myogenic mouse cells [J].
Kuch, C ;
Winnekendonk, D ;
Butz, S ;
Unvericht, U ;
Kemler, R ;
StarzinskiPowitz, A .
EXPERIMENTAL CELL RESEARCH, 1997, 232 (02) :331-338
[32]   DISTINCT MORPHOGENETIC FUNCTIONS OF SIMILAR SMALL GTPASES - DROSOPHILA DRAC1 IS INVOLVED IN AXONAL OUTGROWTH AND MYOBLAST FUSION [J].
LUO, LQ ;
LIAO, YJ ;
JAN, LY ;
JAN, YN .
GENES & DEVELOPMENT, 1994, 8 (15) :1787-1802
[33]   Biogenesis of N-cadherin-dependent cell-cell contacts in living fibroblasts is a microtubule-dependent kinesin-driven mechanism [J].
Mary, S ;
Charrasse, S ;
Meriane, M ;
Comunale, F ;
Travo, P ;
Blangy, A ;
Gauthier-Rouvière, C .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (01) :285-301
[34]   Participation of small GTPases Rac1 and Cdc42Hs in myoblast transformation [J].
Meriane, M ;
Charrasse, S ;
Comunale, F ;
Méry, A ;
Fort, P ;
Roux, P ;
Gauthier-Rouvière, C .
ONCOGENE, 2002, 21 (18) :2901-2907
[35]   Critical activities of Rac1 and Cdc42Hs in skeletal myogenesis:: Antagonistic effects of JNK and p38 pathways [J].
Meriane, M ;
Roux, P ;
Primig, M ;
Fort, P ;
Gauthier-Rouvière, C .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (08) :2513-2528
[36]  
MOORE R, 1993, DEVELOPMENT, V117, P1409
[37]  
Musa H, 2003, J MUSCLE RES CELL M, V24, P301
[38]   Myoblast city, the Drosophila homolog of DOCK180/CED-5, is required in a Rac signaling pathway utilized for multiple developmental processes [J].
Nolan, KM ;
Barrett, K ;
Lu, Y ;
Hu, KQ ;
Vincent, S ;
Settleman, J .
GENES & DEVELOPMENT, 1998, 12 (21) :3337-3342
[39]   p120 catenin regulates the actin cytoskeleton via Rho family GTPases [J].
Noren, NK ;
Liu, BP ;
Burridge, K ;
Kreft, B .
JOURNAL OF CELL BIOLOGY, 2000, 150 (03) :567-579
[40]   Skeletal muscle deformity and neuronal disorder in Trio exchange factor-deficient mouse embryos [J].
O'Brien, SP ;
Seipel, K ;
Medley, QG ;
Bronson, R ;
Segal, R ;
Streuli, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (22) :12074-12078