Masocha Willias
Department of Applied Therapeutics, Faculty of Pharmacy, Kuwait University, Safat, 13110, Kuwait.
J Neuroimmunol. 2009 Sep 29;214(1-2):78-82. doi: 10.1016/j.jneuroim.2009.06.022. Epub 2009 Aug 4.
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.
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。