Chen H C, Chan P C, Tang M J, Cheng C H, Chang T J
Department of Zoology, College of Agriculture, National Chung Hsing University, Taichung, Taiwan, Republic of China.
J Biol Chem. 1998 Oct 2;273(40):25777-82. doi: 10.1074/jbc.273.40.25777.
Focal adhesion kinase (FAK) is a cytoplasmic tyrosine kinase involved in integrin-mediated signal transduction pathway. In this report, we describe that the treatment of hepatocyte growth factor (HGF) stimulates a significant increase in the tyrosine phosphorylation of FAK in human embryonic kidney 293 cells. This stimulation is independent of cell adhesion or the integrity of the actin cytoskeleton, suggesting potentially different mechanisms by which the HGF receptors and integrins regulate the tyrosine phosphorylation of FAK. Our results also suggest that the activation of Src upon HGF stimulation is likely to be one, if not the only, of the mechanisms responsible for the HGF-induced tyrosine phosphorylation of FAK. Furthermore, we showed that a mutation in the Grb2 binding site Tyr-925 of FAK partially abolishes its increase in HGF-induced phosphorylation. Finally, we demonstrated that HGF stimulates the association of FAK with Grb2 in vitro and in intact cells and provided evidence that FAK might contribute to the activation of mitogen-activated protein kinase through Ras in HGF signaling by functioning as an adapter molecule.
粘着斑激酶(FAK)是一种参与整合素介导的信号转导途径的细胞质酪氨酸激酶。在本报告中,我们描述了肝细胞生长因子(HGF)处理可刺激人胚肾293细胞中FAK的酪氨酸磷酸化显著增加。这种刺激与细胞粘附或肌动蛋白细胞骨架的完整性无关,这表明HGF受体和整合素调节FAK酪氨酸磷酸化的潜在机制可能不同。我们的结果还表明,HGF刺激后Src的激活可能是负责HGF诱导的FAK酪氨酸磷酸化的机制之一,如果不是唯一机制的话。此外,我们表明FAK的Grb2结合位点Tyr-925处的突变部分消除了其在HGF诱导的磷酸化中的增加。最后,我们证明HGF在体外和完整细胞中刺激FAK与Grb2的结合,并提供证据表明FAK可能通过作为衔接分子在HGF信号传导中通过Ras促进丝裂原活化蛋白激酶的激活。