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糖原合成酶激酶-3在磷脂酰肌醇3-激酶/Akt细胞存活通路中的作用。

Role of glycogen synthase kinase-3 in the phosphatidylinositol 3-Kinase/Akt cell survival pathway.

作者信息

Pap M, Cooper G M

机构信息

Dana-Farber Cancer Institute and the Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

J Biol Chem. 1998 Aug 7;273(32):19929-32. doi: 10.1074/jbc.273.32.19929.

Abstract

Growth factor-dependent survival of a variety of mammalian cells is dependent on the activation of phosphatidylinositol (PI) 3-kinase and its downstream effector, the protein kinase Akt. Glycogen synthase kinase-3 (GSK-3) has been previously identified as a physiological target of Akt, which is inhibited by phosphorylation, so we have investigated the role of GSK-3 in cell survival. Overexpression of catalytically active GSK-3 induced apoptosis of both Rat-1 and PC12 cells, whereas dominant-negative GSK-3 prevented apoptosis following inhibition of PI 3-kinase. GSK-3 thus plays a critical role in regulation of apoptosis and represents a key downstream target of the PI 3-kinase/Akt survival signaling pathway.

摘要

多种哺乳动物细胞的生长因子依赖性存活取决于磷脂酰肌醇(PI)3激酶及其下游效应物蛋白激酶Akt的激活。糖原合酶激酶-3(GSK-3)先前已被确定为Akt的生理靶点,其通过磷酸化被抑制,因此我们研究了GSK-3在细胞存活中的作用。催化活性GSK-3的过表达诱导了大鼠1细胞和PC12细胞的凋亡,而显性负性GSK-3在PI 3激酶受到抑制后可防止细胞凋亡。因此,GSK-3在细胞凋亡调控中起关键作用,是PI 3激酶/Akt存活信号通路的关键下游靶点。

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