Welsh G I, Foulstone E J, Young S W, Tavaré J M, Proud C G
Department of Biochemistry, School of Medical Sciences, University of Bristol, U.K.
Biochem J. 1994 Oct 1;303 ( Pt 1)(Pt 1):15-20. doi: 10.1042/bj3030015.
We have previously shown that insulin causes inactivation of glycogen synthase kinase-3 (GSK-3) in Chinese hamster ovary cells over-expressing the human insulin receptor (CHO.T cells). We now show that serum and phorbol ester also cause rapid inactivation of GSK-3, both in CHO.T cells and in the nontransfected parental cell line, CHO.K1 cells. Rapamycin was without effect on the inactivation of GSK-3 by insulin, serum or phorbol ester, indicating that the p70 S6 kinase pathway is not involved. In contrast, wortmannin, a potent inhibitor of phosphatidylinositol 3-kinase, blocked the effects of both insulin and serum on GSK-3 activity, and also substantially reduced the activation of both p90 S6 kinase (by insulin) and mitogen-activated protein (MAP) kinase (by insulin and serum). These findings imply (i) that GSK-3 activity is regulated by a cascade involving MAP kinase and p90 S6 kinase and (ii) that wortmannin affects an early step in the MAP kinase pathway. One can infer from this that GSK-3 may be an important regulatory enzyme for the control of several biosynthetic pathways, key enzymes in which are regulated by GSK-3-mediated phosphorylation. Wortmannin had a smaller effect on the activation of MAP kinase by phorbol ester, indicating that phorbol esters may stimulate MAP kinase by a different or additional mechanism to that employed by insulin or serum. Wortmannin had very little effect on the inactivation of GSK-3 by phorbol ester: possible reasons for this are discussed.
我们之前已经表明,胰岛素可使过表达人胰岛素受体的中国仓鼠卵巢细胞(CHO.T细胞)中的糖原合酶激酶-3(GSK-3)失活。我们现在发现,血清和佛波酯也能使GSK-3快速失活,无论是在CHO.T细胞还是未转染的亲本细胞系CHO.K1细胞中。雷帕霉素对胰岛素、血清或佛波酯介导的GSK-3失活没有影响,这表明p70 S6激酶途径未参与其中。相比之下,磷脂酰肌醇3激酶的强效抑制剂渥曼青霉素可阻断胰岛素和血清对GSK-3活性的影响,并且还能显著降低p90 S6激酶(由胰岛素激活)和丝裂原活化蛋白(MAP)激酶(由胰岛素和血清激活)的活性。这些发现表明:(i)GSK-3的活性受涉及MAP激酶和p90 S6激酶的级联反应调控;(ii)渥曼青霉素影响MAP激酶途径的早期步骤。由此可以推断,GSK-3可能是控制多种生物合成途径的重要调节酶,其中的关键酶受GSK-3介导的磷酸化作用调控。渥曼青霉素对佛波酯激活MAP激酶的作用较小,这表明佛波酯可能通过与胰岛素或血清不同或额外的机制来刺激MAP激酶。渥曼青霉素对佛波酯介导的GSK-3失活影响很小,本文讨论了其中可能的原因。