小胶质细胞
促炎细胞因子
肿瘤坏死因子α
实验性自身免疫性脑脊髓炎
受体
生物
细胞生物学
免疫学
神经炎症
多发性硬化
神经科学
炎症
生物化学
作者
Caroline Bouchard,Julie Pagé,Andréanne Bédard,Pierrot Tremblay,Luc Vallières
出处
期刊:Glia
[Wiley]
日期:2007-03-27
卷期号:55 (8): 790-800
被引量:127
摘要
Abstract G protein‐coupled receptor 84 (GPR84) is a recently discovered member of the seven transmembrane receptor superfamily whose function and regulation are unknown. Here, we report that in mice suffering from endotoxemia, microglia express GPR84 in a strong and sustained manner. This property is shared by subpopulations of peripheral macrophages and, to a much lesser extent, monocytes. The induction of GPR84 expression by endotoxin is mediated, at least in part, by proinflammatory cytokines, notably tumor necrosis factor (TNF) and interleukin‐1 (IL‐1), because mice lacking either one or both of these molecules have fewer GPR84‐expressing cells in their cerebral cortex than wild‐type mice during the early phase of endotoxemia. Moreover, when injected intracerebrally or added to microglial cultures, recombinant TNF stimulates GPR84 expression through a dexamethasone‐insensitive mechanism. Finally, we show that microglia produce GPR84 not only during endotoxemia, but also during experimental autoimmune encephalomyelitis (EAE), a model of multiple sclerosis. In conclusion, this study reports the identification of a new sensitive marker of microglial activation, which may play an important regulatory role in neuroimmunological processes, acting downstream to the effects of proinflammatory mediators. © 2007 Wiley‐Liss, Inc.
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