Lyons Anthony, Downer Eric J, Crotty Suzanne, Nolan Yvonne M, Mills Kingston H G, Lynch Marina A
Trinity College Institute for Neuroscience, Physiology Department, Trinity College, Dublin 2, Ireland.
J Neurosci. 2007 Aug 1;27(31):8309-13. doi: 10.1523/JNEUROSCI.1781-07.2007.
Deficits in cognitive function are associated with neuroinflammatory changes, typified by activation of glial cells and an alteration of the pro- and anti-inflammatory cytokine balance in the brain. Although there is evidence to suggest that activation of microglia is regulated by interaction with other cell types in the brain, the mechanism(s) involved is poorly understood. Here, we provide evidence that interaction between CD200 and its receptor plays a role in modulating microglial activation under conditions of chronic and acute inflammation of the brain. We report that interleukin-4 (IL-4) plays a central role in modulating expression of CD200 and identify a mechanism by which IL-4 directly controls microglial cell activation. Our findings provide the first demonstration of a role for IL-4 in modulating CD200 expression and suggest a mechanism for regulation of microglial activation in the intact CNS under inflammatory conditions.
认知功能缺陷与神经炎症变化相关,其典型特征是胶质细胞激活以及大脑中促炎和抗炎细胞因子平衡的改变。尽管有证据表明小胶质细胞的激活受其与大脑中其他细胞类型相互作用的调节,但其中涉及的机制仍知之甚少。在此,我们提供证据表明,CD200与其受体之间的相互作用在调节大脑慢性和急性炎症条件下的小胶质细胞激活中发挥作用。我们报告白细胞介素-4(IL-4)在调节CD200表达中起核心作用,并确定了IL-4直接控制小胶质细胞激活的机制。我们的研究结果首次证明了IL-4在调节CD200表达中的作用,并提出了在炎症条件下完整中枢神经系统中调节小胶质细胞激活的机制。