The atypical Rho family GTPase Wrch-1 regulates focal adhesion formation and cell migration

被引:40
作者
Chuang, Ya-Yu
Valster, Aline
Coniglio, Salvatore J.
Backer, Jonathan M.
Symons, Marc [1 ]
机构
[1] N Shore Univ Hosp, Feinstein Inst Med Res, Ctr Oncol & Cell Biol, N Shore LIJ, Manhasset, NY 11030 USA
[2] Albert Einstein Coll Med, Dept Anat & Struct Biol, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Dept Mol Pharmacol, Bronx, NY 10461 USA
[4] N Shore Univ Hosp, Dept Surg, Manhasset, NY 11030 USA
关键词
Wrch-1; Rho; focal adhesion; cell migration; myosin;
D O I
10.1242/jcs.03456
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Wrch-1 (Wnt-regulated Cdc42 homolog) is a new member of the Rho family that was identified as a gene transcriptionally upregulated by Wnt-1. Wrch-1 has no detectable GTPase activity and displays very high intrinsic guanine nucleotide exchange, implying that it is constitutively GTP-bound. The biological functions of Wrch-1 largely remain to be characterized. Here, we report that Wrch-1 prominently localizes to focal adhesions. Depletion of Wrch-1 by small interfering RNA increases focal adhesion formation, whereas Wrch-1 overexpression disassembles focal adhesions. Wrch-1 depletion inhibits myosin-light-chain phosphorylation, which in turn leads to an increase in the number of focal adhesions and inhibits cell migration in response to wound healing. Depletion of Wrch-1 also inhibits Akt and JNK activation. Although pharmacological inhibitors of Akt and JNK inhibit cell migration, they do not affect focal adhesions. Thus, our data suggest that Wrch-1 regulates cell migration by multiple mechanisms: on the one hand Wrch-1 controls focal adhesions by regulating myosin light chain and on the other hand Wrch-1 stimulates the activation of Akt and JNK.
引用
收藏
页码:1927 / 1934
页数:8
相关论文
共 38 条
  • [1] Matrix survival signaling:: From fibronectin via focal adhesion kinase to c-Jun NH2-terminal kinase
    Almeida, EAC
    Ilic, D
    Han, Q
    Hauck, CR
    Jin, F
    Kawakatsu, H
    Schlaepfer, DD
    Damsky, CH
    [J]. JOURNAL OF CELL BIOLOGY, 2000, 149 (03) : 741 - 754
  • [2] Rho GTPases have diverse effects on the organization of the actin filament system
    Aspenström, P
    Fransson, Å
    Saras, J
    [J]. BIOCHEMICAL JOURNAL, 2004, 377 : 327 - 337
  • [3] Transforming activity of the Rho family GTPase, Wrch-1, a Wnt-regulated Cdc42 homolog, is dependent on a novel carboxyl-terminal palmitoylation motif
    Berzat, AC
    Buss, JE
    Chenette, EJ
    Weinbaum, CA
    Shutes, A
    Der, CJ
    Minden, A
    Cox, AD
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (38) : 33055 - 33065
  • [4] Rho and Rac take center stage
    Burridge, K
    Wennerberg, K
    [J]. CELL, 2004, 116 (02) : 167 - 179
  • [5] Focal adhesions, contractility, and signaling
    Burridge, K
    ChrzanowskaWodnicka, M
    [J]. ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1996, 12 : 463 - 518
  • [6] Roles of the Rac1 and Rac3 GTPases in human tumor cell invasion
    Chan, AY
    Coniglio, SJ
    Chuang, YY
    Michaelson, D
    Knaus, UG
    Philips, MR
    Symons, M
    [J]. ONCOGENE, 2005, 24 (53) : 7821 - 7829
  • [7] Phosphorylation of non-muscle myosin II regulatory light chain by p21-activated kinase (γ-PAK)
    Chew, TL
    Masaracchia, RA
    Goeckeler, ZM
    Wysolmerski, RB
    [J]. JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY, 1998, 19 (08) : 839 - 854
  • [8] Essential role of non-canonical Wnt signalling in neural crest migration
    De Calisto, J
    Araya, C
    Marchant, L
    Riaz, CF
    Mayor, R
    [J]. DEVELOPMENT, 2005, 132 (11): : 2587 - 2597
  • [9] Wnt-3a-dependent cell motility involves RhoA activation and is specifically regulated by dishevelled-2
    Endo, Y
    Wolf, V
    Muraiso, K
    Kamijo, K
    Soon, L
    Üren, A
    Barshishat-Küpper, M
    Rubin, JS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (01) : 777 - 786
  • [10] N-terminal domains of the class IA phosphoinositide 3-kinase regulatory subunit play a role in cytoskeletal but not mitogenic signaling
    Hill, KM
    Huang, YH
    Yip, SC
    Yu, JH
    Segall, JE
    Backer, JM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (19) : 16374 - 16378