Abbi Smita, Ueda Hiroki, Zheng Chuanhai, Cooper Lee Ann, Zhao Jihe, Christopher Renee, Guan Jun-Lin
Department of Molecular Medicine, College of Veterinary Medicine, Cornell University, Ithaca, New York 14853, USA.
Mol Biol Cell. 2002 Sep;13(9):3178-91. doi: 10.1091/mbc.e02-05-0295.
Focal adhesion kinase (FAK) is a major mediator of integrin signaling pathways. The mechanisms of regulation of FAK activity and its associated cellular functions are not very well understood. Here, we present data suggesting that a novel protein FIP200 functions as an inhibitor for FAK. We show the association of endogenous FIP200 with FAK, which is decreased upon integrin-mediated cell adhesion concomitant with FAK activation. In vitro- and in vivo-binding studies indicate that FIP200 interacts with FAK through multiple domains directly. FIP200 bound to the kinase domain of FAK inhibited its kinase activity in vitro and its autophosphorylation in vivo. Overexpression of FIP200 or its segments inhibited cell spreading, cell migration, and cell cycle progression, which correlated with their inhibition of FAK activity in vivo. The inhibition of these cellular functions by FIP200 could be rescued by coexpression of FAK. Last, we show that disruption of the functional interaction between endogenous FIP200 with FAK leads to increased FAK phosphorylation and partial restoration of cell cycle progression in cells plated on poly-L-lysine, providing further support for FIP200 as a negative regulator of FAK. Together, these results identify FIP200 as a novel protein inhibitor for FAK.
粘着斑激酶(FAK)是整合素信号通路的主要介导因子。目前对FAK活性调控机制及其相关细胞功能的了解还不是很清楚。在此,我们提供的数据表明一种新型蛋白质FIP200作为FAK的抑制剂发挥作用。我们展示了内源性FIP200与FAK的关联,在整合素介导的细胞黏附伴随FAK激活时这种关联会减弱。体外和体内结合研究表明,FIP200通过多个结构域直接与FAK相互作用。与FAK激酶结构域结合的FIP200在体外抑制其激酶活性,在体内抑制其自身磷酸化。FIP200或其片段的过表达抑制细胞铺展、细胞迁移和细胞周期进程,这与它们在体内对FAK活性的抑制相关。FAK的共表达可以挽救FIP200对这些细胞功能的抑制。最后,我们表明内源性FIP200与FAK之间功能相互作用的破坏导致FAK磷酸化增加以及在聚-L-赖氨酸包被的细胞中细胞周期进程部分恢复,这进一步支持FIP200作为FAK的负调控因子。总之,这些结果确定FIP200是一种新型的FAK蛋白质抑制剂。