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Published online 20 May 2002. doi:10.1083/jcb.200112107
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© The Rockefeller University Press, 0021-9525/2002/5/819 $5.00
The Journal of Cell Biology, Volume 157, Number 5, May 28, 2002 819-830


Article

ROCK and mDia1 antagonize in Rho-dependent Rac activation in Swiss 3T3 fibroblasts



Takahiro Tsuji1, Toshimasa Ishizaki1, Muneo Okamoto1, Chiharu Higashida1, Kazuhiro Kimura1, Tomoyuki Furuyashiki1, Yoshiki Arakawa1, Raymond B. Birge2, Tetsuya Nakamoto3, Hisamaru Hirai3 and Shuh Narumiya1

1 Department of Pharmacology, Kyoto University Faculty of Medicine, Kyoto 606-8501, Japan
2 Department of Biochemistry and Molecular Biology, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, NJ 07214
3 Department of Hematology and Oncology, Faculty of Medicine, University of Tokyo, Tokyo 113-8655, Japan

Address correspondence to Shuh Narumiya, Dept. of Pharmacology, Kyoto University Faculty of Medicine, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan. Tel.: 81-75-753-4392. Fax: 81-75-753-4693. E-mail: snaru{at}mfour.med.kyoto-u.ac.jp

The small GTPase Rho acts on two effectors, ROCK and mDia1, and induces stress fibers and focal adhesions. However, how ROCK and mDia1 individually regulate signals and dynamics of these structures remains unknown. We stimulated serum-starved Swiss 3T3 fibroblasts with LPA and compared the effects of C3 exoenzyme, a Rho inhibitor, with those of Y-27632, a ROCK inhibitor. Y-27632 treatment suppressed LPA-induced formation of stress fibers and focal adhesions as did C3 exoenzyme but induced membrane ruffles and focal complexes, which were absent in the C3 exoenzyme-treated cells. This phenotype was suppressed by expression of N17Rac. Consistently, the amount of GTP-Rac increased significantly by Y-27632 in LPA-stimulated cells. Biochemically, Y-27632 suppressed tyrosine phosphorylation of paxillin and focal adhesion kinase and not that of Cas. Inhibition of Cas phosphorylation with PP1 or expression of a dominant negative Cas mutant inhibited Y-27632–induced membrane ruffle formation. Moreover, Crk-II mutants lacking in binding to either phosphorylated Cas or DOCK180 suppressed the Y-27632–induced membrane ruffle formation. Finally, expression of a dominant negative mDia1 mutant also inhibited the membrane ruffle formation by Y-27632. Thus, these results have revealed the Rho-dependent Rac activation signaling that is mediated by mDia1 through Cas phosphorylation and antagonized by the action of ROCK.

Key Words: Rho; mDia; Rac; membrane ruffles; Y-27632


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