Role of p38 and p44/42 mitogen-activated protein kinases in microglia

被引:243
作者
Koistinaho, M
Koistinaho, J
机构
[1] Univ Kuopio, AI Virtanen Inst Mol Sci, Dept Neurobiol, FIN-70211 Kuopio, Finland
[2] Kuopio Univ Hosp, Dept Clin Pathol, SF-70210 Kuopio, Finland
关键词
inflammation; cytokines; brain ischemia; Alzheimer's disease;
D O I
10.1002/glia.10151
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although microglial cells are thought to play a beneficial role in the regeneration and plasticity of the central nervous system (CNS), recent studies have indicated that at least some molecules released by microglia may be harmful in acute brain insults and neurodegenerative diseases. Therefore, the pathways mediating the synthesis and release of these neurotoxic compounds are of importance. p38 and p44/42 families of mitogen-activated protein kinases (MAPKs) in microglia respond strongly to various extracellular stimuli, such as ATP, thrombin, and beta-amyloid, a peptide thought to be responsible for the neuropathology in Alzheimer's disease. In this review we describe in vivo evidence implicating that p38 and p44/42 MAPKs may play a critical role in harmful microglial activation in acute brain injury, such as stroke, and in more chronic neurodegenerative diseases, such as Alzheimer's disease. We also clarify the extracellular signals responsible for activation of p38 and p44/42 MAPK in microglia and review the responses so far reported to be mediated by these kinases. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:175 / 183
页数:9
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