Rho GTPases control polarity, protrusion, and adhesion during cell movement

被引:1196
作者
Nobes, CD
Hall, A
机构
[1] UCL, MRC, Mol Cell Biol Lab, CRC Oncogene & Signal Transduct Grp, London WC1E 6BT, England
[2] UCL, Dept Biochem, London WC1E 6BT, England
关键词
Rho GTPases; Ras; polarity; focal adhesion; wound healing;
D O I
10.1083/jcb.144.6.1235
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell movement is essential during embryogenesis to establish tissue patterns and to drive morphogenetic pathways and in the adult for tissue repair and to direct cells to sites of infection. Animal cells move by crawling and the driving force is derived primarily from the coordinated assembly and disassembly of actin filaments. The small GTPases, Rho, Rac, and Cdc42, regulate the organization of actin filaments and we have analyzed their contributions to the movement of primary embryo fibroblasts in an in vitro wound healing assay. Rac is essential for the protrusion of lamellipodia and for forward movement. Cdc42 is required to maintain cell polarity, which includes the localization of lamellipodial activity to the leading edge and the reorientation of the Golgi apparatus in the direction of movement. Rho is required to maintain cell adhesion during movement, but stress fibers and focal adhesions are not required. Finally, Ras regulates focal adhesion and stress fiber turnover and this is essential for cell movement. We conclude that the signal transduction pathways controlled by the four small GTPases, Rho, Rac, Cdc42, and Ras, cooperate to promote cell movement.
引用
收藏
页码:1235 / 1244
页数:10
相关论文
共 66 条
[11]   Origins of cell polarity [J].
Drubin, DG ;
Nelson, WJ .
CELL, 1996, 84 (03) :335-344
[12]  
DUNLEVY JR, 1993, J CELL SCI, V105, P489
[13]  
Dunn GA., 1980, Cell Adhes. Mot, P409
[14]   PHOSPHORYLATION OF GAP AND GAP-ASSOCIATED PROTEINS BY TRANSFORMING AND MITOGENIC TYROSINE KINASES [J].
ELLIS, C ;
MORAN, M ;
MCCORMICK, F ;
PAWSON, T .
NATURE, 1990, 343 (6256) :377-381
[15]   MECHANISM OF CENTROSOME POSITIONING DURING THE WOUND RESPONSE IN BSC-1 CELLS [J].
EUTENEUER, U ;
SCHLIWA, M .
JOURNAL OF CELL BIOLOGY, 1992, 116 (05) :1157-1166
[16]  
FOX PL, 1994, ONCOGENE, V9, P3519
[17]   MONOCLONAL-ANTIBODIES TO THE P21 PRODUCTS OF THE TRANSFORMING GENE OF HARVEY MURINE SARCOMA-VIRUS AND OF THE CELLULAR RAS GENE FAMILY [J].
FURTH, ME ;
DAVIS, LJ ;
FLEURDELYS, B ;
SCOLNICK, EM .
JOURNAL OF VIROLOGY, 1982, 43 (01) :294-304
[18]   Inhibition of focal adhesion kinase (FAK) signaling in focal adhesions decreases cell motility and proliferation [J].
Gilmore, AP ;
Romer, LH .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (08) :1209-1224
[19]   Coupling of Jun amino-terminal kinase and decapentaplegic in Drosophila morphogenesis [J].
Glise, B ;
Noselli, S .
GENES & DEVELOPMENT, 1997, 11 (13) :1738-1747
[20]   MICROTUBULE-ORGANIZING CENTERS AND CELL-MIGRATION - EFFECT OF INHIBITION OF MIGRATION AND MICROTUBULE DISRUPTION IN ENDOTHELIAL-CELLS [J].
GOTLIEB, AI ;
SUBRAHMANYAN, L ;
KALNINS, VI .
JOURNAL OF CELL BIOLOGY, 1983, 96 (05) :1266-1272