Signaling by reactive oxygen species in the nervous system

被引:160
作者
Maher, P
Schubert, D
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[2] Salk Inst Biol Studies, Cellular Neurobiol Lab, La Jolla, CA 92037 USA
关键词
ROS; apoptosis; necrosis; glutathione; H2O2; transcription factors; tyrosine phosphatases; protein kinases;
D O I
10.1007/PL00000766
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Free radicals and reactive oxygen species (ROS) are involved in a variety of different cellular processes ranging from apoptosis and necrosis to cell proliferation and carcinogenesis. Cells contain multiple sites for ROS production and a few mechanisms for their degradation. Which of these sites is activated by a given stimulus may play a role in dictating the subsequent downstream effects of the ROS generated on cellular function. Even when the ultimate outcome is similar, such as when ROS production leads to cell death, the specific cellular changes can be quite different depending on the initial stimulus and the type of cell involved. These data, along with the evidence that ROS can modify a number of intracellular signaling pathways including protein phosphatases, protein kinases and transcription factors, suggest that the majority of the effects of ROS on cells are through their actions on signaling pathways rather than via nonspecific damage of intracellular macromolecules.
引用
收藏
页码:1287 / 1305
页数:19
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