Susa M, Olivier A R, Fabbro D, Thomas G
Friedrich Miescher Institut, Basel, Switzerland.
Cell. 1989 Jun 2;57(5):817-24. doi: 10.1016/0092-8674(89)90796-4.
Detailed kinetics reveal that EGF-induced S6 kinase activation is biphasic: an early phase appears at 10-15 min, followed by a late phase between 30 and 60 min. Both activities exhibit the same chromatographic behavior and sensitivity to phosphatase 2A. Direct activation of protein kinase C by TPA induces only late phase activity. Down-regulation of protein kinase C leads to loss of both TPA- and EGF-induced late phase activity, while the early phase is unaffected. The loss of late phase kinase activity results in decreased EGF-induced S6 phosphorylation, protein synthesis, and cell growth. The results indicate that EGF differentially regulates S6 kinase activation by two distinct signaling pathways and that loss of the late or protein kinase C-dependent phase leads to a diminished mitogenic response.
详细的动力学研究表明,表皮生长因子(EGF)诱导的S6激酶激活是双相的:早期阶段出现在10 - 15分钟,随后晚期阶段出现在30至60分钟之间。两种活性表现出相同的色谱行为以及对磷酸酶2A的敏感性。佛波酯(TPA)直接激活蛋白激酶C仅诱导晚期活性。蛋白激酶C的下调导致TPA和EGF诱导的晚期活性丧失,而早期活性不受影响。晚期激酶活性的丧失导致EGF诱导的S6磷酸化、蛋白质合成和细胞生长减少。结果表明,EGF通过两种不同的信号通路差异性地调节S6激酶激活,并且晚期或蛋白激酶C依赖性阶段的丧失导致有丝分裂反应减弱。