Polk D B
Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Gastroenterology. 1995 Dec;109(6):1845-51. doi: 10.1016/0016-5085(95)90751-3.
BACKGROUND & AIMS: Epidermal growth factor (EGF) has been shown to induce intestinal proliferation and maturation; however, little information is available regarding substrates of the intestinal EGF receptor tyrosine kinase. The purpose of this study was to determine if src homologous collagen-like protein (Shc) was an in vivo substrate of the intestinal EGF receptor.
Ten-day-old rats were treated with EGF or were breast-fed. In some experiments, IEC-6 cells were treated with EGF. Intestinal tissue and cell fractions were studied by immunodetection to compare the tyrosine phosphorylation state and the subcellular localization of intestinal proteins.
The total tyrosine phosphorylation state of intestinal proteins was increased threefold by EGF. Tyrosine phosphorylation of the EGF receptor and Shc were rapidly increased by EGF. The association of Grb2 with Shc increased fourfold and fivefold. Plasma membrane translocation of Shc and associated phosphotyrosyl proteins was increased within 30 seconds of EGF treatment.
Shc is a substrate of the intestinal EGF receptor in vivo. EGF-induced association of Shc with the adapter protein Grb2 may have implications for activation of the p21ras signaling pathway in the intestine. The EGF-induced membrane association of Shc with two other phosphotyrosyl proteins suggests involvement of Shc in additional aspects of EGF-receptor signaling in the intestine.
表皮生长因子(EGF)已被证明可诱导肠道增殖和成熟;然而,关于肠道表皮生长因子受体酪氨酸激酶的底物的信息却很少。本研究的目的是确定src同源胶原样蛋白(Shc)是否为肠道表皮生长因子受体的体内底物。
对10日龄大鼠给予EGF治疗或母乳喂养。在一些实验中,用EGF处理IEC-6细胞。通过免疫检测研究肠道组织和细胞组分,以比较肠道蛋白的酪氨酸磷酸化状态和亚细胞定位。
EGF使肠道蛋白的总酪氨酸磷酸化状态增加了三倍。EGF使表皮生长因子受体和Shc的酪氨酸磷酸化迅速增加。Grb2与Shc的结合增加了四倍和五倍。在EGF处理后30秒内,Shc和相关磷酸酪氨酸蛋白的质膜转位增加。
Shc是肠道表皮生长因子受体的体内底物。EGF诱导的Shc与衔接蛋白Grb2的结合可能对肠道中p21ras信号通路的激活有影响。EGF诱导的Shc与另外两种磷酸酪氨酸蛋白的膜结合表明Shc参与了肠道表皮生长因子受体信号传导的其他方面。