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磷脂酰肌醇-3激酶在钒酸盐促进S期进入中的作用。

The role of phosphatidylinositol-3 kinase in vanadate-promoted S phase entry.

作者信息

Zhang Zhuo, Gao Ning, He Hengjun, Huang Chuanshu, Jiang Bing-hua, Jia Luo, Shi Xianglin

机构信息

Pathology and Physiology Research Branch, National Institute for Occupational Safety and Health, Morgantown, WV 26505, USA.

出版信息

Mol Cell Biochem. 2004 Jan;255(1-2):239-45. doi: 10.1023/b:mcbi.0000007279.28280.e5.

Abstract

Phosphatidylinositil-3 kinase (PI3K) is a heterodimer of catalytic and regulatory subunits. It is involved in various signaling pathways and key functions of the cells. The present study investigated the role of PI3K in vanadate-induced alteration in cell cycle regulation in C141 mouse epidermal cells. Vanadate caused a time- and dose-dependent increase in PI3K activity and phosphorylation of p70 S6 kinase (p70S6K) at Thr421/Ser424 and Thr389 sites. The phosphorylation at these sites was inhibited by PI3K inhibitor, LY294002, and p70S6K mutation. Vanadate promoted S phase entry and this promotion was inhibited by LY294002 and rapmycin, a p70S6K inhibitor. Vanadate-induced enhancement in S phase entry was also inhibited in transfection with dominant negative p70S6K mutant cells. The results obtained show that vanadate is able to increase PI3K activity through phosphorylation. PI3K activated p70S6K, which phosphated protein S6, and promoted S phase entry.

摘要

磷脂酰肌醇-3激酶(PI3K)是一种由催化亚基和调节亚基组成的异二聚体。它参与细胞的各种信号通路和关键功能。本研究调查了PI3K在钒酸盐诱导的C141小鼠表皮细胞周期调控改变中的作用。钒酸盐导致PI3K活性以及p70 S6激酶(p70S6K)在苏氨酸421/丝氨酸424和苏氨酸389位点的磷酸化呈时间和剂量依赖性增加。这些位点的磷酸化受到PI3K抑制剂LY294002和p70S6K突变的抑制。钒酸盐促进S期进入,而这种促进作用受到LY294002和雷帕霉素(一种p70S6K抑制剂)的抑制。在转染显性负性p70S6K突变细胞中,钒酸盐诱导的S期进入增强也受到抑制。所得结果表明,钒酸盐能够通过磷酸化增加PI3K活性。PI3K激活p70S6K,后者使蛋白S6磷酸化,并促进S期进入。

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