Purinergic (P2X7) receptor activation of microglia induces cell death via an interleukin-1-independent mechanism

被引:115
作者
Brough, D [1 ]
Le Feuvre, RA
Iwakura, Y
Rothwell, NJ
机构
[1] Univ Manchester, Sch Biol Sci, Div Neurosci, Manchester M13 9PT, Lancs, England
[2] Univ Tokyo, Inst Med Sci, Lab Anim Res Ctr, Tokyo, Japan
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
D O I
10.1006/mcne.2001.1054
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Activation of purinergic P2X7 receptors, principally by extracellular ATP, promotes the processing and release of the cytokine interleukin-1beta(IL-1beta) and induces cell death in activated microglia and macrophages. The objective of this study was to determine if IL-1beta release contributes directly to this cell death in microglia. Exposure of microglia to bacterial lipopolysaccharide (LPS) and ATP induced release of IL-1beta and IL-1alpha, as well as cell death. Neither cell death nor IL-1 release was observed in microglia lacking the P2X7 receptor. Microglia from mice lacking the IL-1beta gene demonstrated a profile of death identical to that of wild-type microglia in response to LPS and ATP. Thus, IL-1beta is not required for P2X7 receptor-stimulated microglial death.
引用
收藏
页码:272 / 280
页数:9
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