Kaibuchi K, Kuroda S, Fukata M, Nakagawa M
Division of Signal Transduction Nara Institute of Science and Technology 8916-5, Takayama, Ikoma, 630-0101, Japan. kaibuchi@bs. aist-nara.ac.jp.
Curr Opin Cell Biol. 1999 Oct;11(5):591-6. doi: 10.1016/s0955-0674(99)00014-9.
Reports in the past two years have shown that Cdc42, Rac1, and Rho - belonging to the Rho small GTPase family - participate in the regulation of cadherin-mediated cell-cell adhesion. IQGAP1, an effector of Cdc42 and Rac1, interacts with cadherin and beta-catenin and induces the dissociation of alpha-catenin from the cadherin-catenins complex leading to disruption of cell-cell adhesion: activated Cdc42 and Rac1 counteract the effect of IQGAP1. Thus, Cdc42 and Rac1 appear to regulate cadherin-mediated cell-cell adhesion acting through IQGAP1.
过去两年的报告显示,属于Rho小GTP酶家族的Cdc42、Rac1和Rho参与了钙黏蛋白介导的细胞间黏附的调控。IQGAP1是Cdc42和Rac1的效应器,它与钙黏蛋白和β-连环蛋白相互作用,并诱导α-连环蛋白从钙黏蛋白-连环蛋白复合物中解离,导致细胞间黏附的破坏:活化的Cdc42和Rac1可抵消IQGAP1的作用。因此,Cdc42和Rac1似乎通过IQGAP1来调节钙黏蛋白介导的细胞间黏附。