Uddin S, Yenush L, Sun X J, Sweet M E, White M F, Platanias L C
Division of Hematology-Oncology, Loyola University of Chicago, Maywood, Illinois 60153, USA.
J Biol Chem. 1995 Jul 7;270(27):15938-41. doi: 10.1074/jbc.270.27.15938.
Interferon-alpha (IFN alpha) induces rapid tyrosine phosphorylation of the insulin receptor substrate-1 (IRS-1), a docking protein with multiple tyrosine phosphorylation sites that bind to the Src homology 2 (SH2) domains of various signaling proteins. During IFN alpha stimulation, the p85 regulatory subunit of the phosphatidylinositol 3'-kinase binds via its SH2 domains to tyrosine-phosphorylated IRS-1, and phosphatidylinositol 3'-kinase activity is detected in association with IRS-1. Thus, IFN alpha responses occur by activation of the IRS signaling system, which it shares with insulin, insulin-like growth factor-1, and interleukin-4.
α干扰素(IFNα)可诱导胰岛素受体底物1(IRS-1)快速发生酪氨酸磷酸化,IRS-1是一种具有多个酪氨酸磷酸化位点的对接蛋白,可与多种信号蛋白的Src同源2(SH2)结构域结合。在IFNα刺激过程中,磷脂酰肌醇3'-激酶的p85调节亚基通过其SH2结构域与酪氨酸磷酸化的IRS-1结合,并检测到与IRS-1相关的磷脂酰肌醇3'-激酶活性。因此,IFNα反应是通过激活IRS信号系统而发生的,该信号系统与胰岛素、胰岛素样生长因子-1和白细胞介素-4所共有的。