Kang Ung Gu, Seo Myoung Suk, Roh Myoung-Sun, Kim Yeni, Yoon Se Chang, Kim Yong Sik
Department of Psychiatry and Behavioral Science, Seoul National University College of Medicine, 28 Yongon-Dong, Chongno-Gu, Seoul 110-799, South Korea.
FEBS Lett. 2004 Feb 27;560(1-3):115-9. doi: 10.1016/S0014-5793(04)00082-1.
We investigated the effect of 10 microM clozapine on the activity of glycogen synthase kinase-3beta (GSK-3beta) and its upstream and downstream molecules in SH-SY5Y human neuroblastoma cells. Clozapine activates both Akt- and Dvl-mediated phosphorylation of GSK-3beta through phosphorylation at Ser9, and increased total cellular and intranuclear levels of beta-catenin. Pretreatment with the specific inhibitor of the phosphatidylinositol 3-kinase (PI3K)-Akt pathway, LY294002 (20 microM), prevented the phosphorylation of Akt but did not affect the phosphorylation of GSK-3beta. These results suggest that clozapine regulates the phosphorylation of GSK-3beta through Wnt signal pathways involving Dvl upstream but not through the PI3K-Akt pathway in SH-SY5Y cells.
我们研究了10微摩尔氯氮平对SH-SY5Y人神经母细胞瘤细胞中糖原合酶激酶-3β(GSK-3β)及其上下游分子活性的影响。氯氮平通过Ser9位点的磷酸化激活Akt和Dvl介导的GSK-3β磷酸化,并增加细胞内和细胞核内β-连环蛋白的总量。用磷脂酰肌醇3激酶(PI3K)-Akt途径的特异性抑制剂LY294002(20微摩尔)预处理可阻止Akt的磷酸化,但不影响GSK-3β的磷酸化。这些结果表明,氯氮平通过涉及上游Dvl的Wnt信号通路而非PI3K-Akt途径调节SH-SY5Y细胞中GSK-3β的磷酸化。