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全身脂多糖(LPS)诱导的小胶质细胞激活导致大脑中CD200和CD200受体基因表达在不同时间的降低。

Systemic lipopolysaccharide (LPS)-induced microglial activation results in different temporal reduction of CD200 and CD200 receptor gene expression in the brain.

作者信息

Masocha Willias

机构信息

Department of Applied Therapeutics, Faculty of Pharmacy, Kuwait University, Safat, 13110, Kuwait.

出版信息

J Neuroimmunol. 2009 Sep 29;214(1-2):78-82. doi: 10.1016/j.jneuroim.2009.06.022. Epub 2009 Aug 4.

Abstract

LPS activates microglia, which are normally maintained in a quiescent state by CD200-CD200 receptor (CD200R) interaction. MAC-1 (a microglia marker) mRNA expression was increased in mice brains up to 1 year post LPS administration (i.p.). Minocycline treatment did not prevent LPS (5 mg/kg)-induced increase in MAC-1 mRNA but reduced that induced by 0.1 mg/kg LPS. CD200R mRNA decreased starting at 4 h, whereas CD200 mRNA increased at 4 h and decreased at 1 year post LPS inoculation. Thus, LPS-induced changes in CD200-CD200R equilibrium might keep microglia chronically activated. Minocycline does not effectively inhibit microglia activation induced by high-dose LPS.

摘要

脂多糖(LPS)可激活小胶质细胞,而小胶质细胞通常通过CD200 - CD200受体(CD200R)相互作用维持在静止状态。腹腔注射LPS后长达1年,小鼠脑内MAC - 1(一种小胶质细胞标志物)mRNA表达增加。米诺环素治疗不能预防LPS(5毫克/千克)诱导的MAC - 1 mRNA增加,但可减少0.1毫克/千克LPS诱导的增加。LPS接种后4小时开始,CD200R mRNA减少,而CD200 mRNA在4小时增加,并在1年后减少。因此,LPS诱导的CD200 - CD200R平衡变化可能使小胶质细胞长期激活。米诺环素不能有效抑制高剂量LPS诱导的小胶质细胞激活。

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