Garcia-Guzman M, Larsen E, Vuori K
Cancer Research Center, The Burnham Institute, 10901 North Torrey Pines Road, La Jolla, California, CA 92037, USA.
Oncogene. 2000 Aug 17;19(35):4058-65. doi: 10.1038/sj.onc.1203750.
Hepatocyte growth factor triggers a complex biological program leading to invasive cell growth by activating the c-Met receptor tyrosine kinase. Following activation, Met signaling is elicited via its interactions with SH2-containing proteins, or via the phosphorylation of the docking protein Gab1, and the subsequent interaction of Gab1 with additional SH2-containing effector molecules. We have previously shown that the interaction between phosphorylated Gab1 and the adaptor protein Crk mediates activation of the JNK pathway downstream of Met. We report here that c-Cbl, which is a Gab1-like docking protein, also becomes tyrosine-phosphorylated in response to Met activation and serves as a docking molecule for various SH2-containing molecules, including Crk. We further show that Cbl is similarly capable of enhancing Met-induced JNK activation, and several lines of experimentation suggests that it does so by interacting with Crk. We also show that both Cbl and Gab1 enhance Met-induced activation of another MAP kinase cascade, the ERK pathway, in a Crk-independent manner. Taken together, our studies demonstrate a previously unidentified functional role for Cbl in Met signaling and suggest that Met utilizes at least two docking proteins, Gab1 and Cbl, to activate downstream signaling pathways. Oncogene (2000) 19, 4058 - 4065.
肝细胞生长因子通过激活c-Met受体酪氨酸激酶触发一个复杂的生物学程序,导致侵袭性细胞生长。激活后,Met信号通过其与含SH2结构域蛋白的相互作用,或通过对接蛋白Gab1的磷酸化以及随后Gab1与其他含SH2结构域效应分子的相互作用而引发。我们之前已经表明,磷酸化的Gab1与衔接蛋白Crk之间的相互作用介导了Met下游JNK途径的激活。我们在此报告,c-Cbl作为一种类似于Gab1的对接蛋白,在Met激活时也会发生酪氨酸磷酸化,并作为包括Crk在内的各种含SH2结构域分子的对接分子。我们进一步表明,Cbl同样能够增强Met诱导的JNK激活,并且多项实验表明它是通过与Crk相互作用来实现的。我们还表明,Cbl和Gab1均以不依赖Crk的方式增强Met诱导的另一个MAP激酶级联反应——ERK途径的激活。综上所述,我们的研究证明了Cbl在Met信号传导中以前未被识别的功能作用,并表明Met利用至少两种对接蛋白Gab1和Cbl来激活下游信号通路。《癌基因》(2000年)第19卷,第4058 - 4065页