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氧化还原调节的细胞凋亡信号传导中的应激反应蛋白激酶

Stress-responsive protein kinases in redox-regulated apoptosis signaling.

作者信息

Matsuzawa Atsushi, Ichijo Hidenori

机构信息

Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

出版信息

Antioxid Redox Signal. 2005 Mar-Apr;7(3-4):472-81. doi: 10.1089/ars.2005.7.472.

Abstract

Both extra- and intracellular stimuli elicit a wide variety of responses, such as cell survival, proliferation, differentiation, and apoptosis, through regulation of cell signaling. Recent studies have revealed that stress-responsive signal transduction pathways are strictly regulated by the intracellular redox state. The redox state of the cell is a consequence of the precise balance between the levels of oxidizing and reducing equivalents, such as reactive oxygen species (ROS) and endogenous antioxidants. The generation of ROS fluctuates in response to alterations of both external and internal environment and, in turn, triggers specific signaling cascades, including mitogen-activated protein kinases, which determine cell survival or cell death. This review focuses on the regulatory mechanisms of stress-responsive protein kinases and their involvement in oxidative stress-induced apoptosis. It also provides recent findings on the molecular mechanisms by which redox signaling cross-talks with stress-responsive protein kinase cascades.

摘要

细胞外和细胞内刺激均通过调节细胞信号传导引发多种反应,如细胞存活、增殖、分化和凋亡。最近的研究表明,应激反应信号转导通路受到细胞内氧化还原状态的严格调控。细胞的氧化还原状态是氧化和还原当量(如活性氧(ROS)和内源性抗氧化剂)水平精确平衡的结果。ROS的产生会随着外部和内部环境的变化而波动,进而触发特定的信号级联反应,包括丝裂原活化蛋白激酶,这些反应决定细胞的存活或死亡。本综述重点关注应激反应蛋白激酶的调控机制及其在氧化应激诱导的细胞凋亡中的作用。它还提供了关于氧化还原信号与应激反应蛋白激酶级联相互作用的分子机制的最新研究结果。

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