Flavin M P, Zhao G, Ho L T
Department of Pediatrics, Queen's University, Kingston, Ontario, Canada.
Glia. 2000 Feb 15;29(4):347-54.
Several CNS disorders feature microglial activation. Microglia are known to have both restorative and cytotoxic capabilities. Neuronal apoptosis has been noted after an acute insult such as ischemia. Microglia may participate in this event. We previously showed that conditioned medium (CM) harvested from peritoneal macrophages or from activated microglia triggered apoptosis in rat hippocampal neurons in culture. We wished to characterize the factor responsible for triggering neuronal death. Quiescent microglia produced CM that did not disrupt hippocampal neurons. Lipopolysaccharide-activated microglia produced CM which resulted in neuronal death. This effect was blocked by plasminogen activator inhibitor-1, by tPA STOP, and by co-incubation with tPA antibody. Recombinant human tPA exaggerated the neurotoxic effects of microglial CM, while tPA alone was toxic only at very high concentrations. This in vitro system, which probably excludes any significant impact of microglial free radicals, suggests that microglial tPA may contribute significantly to hippocampal neuronal death.
几种中枢神经系统疾病的特征是小胶质细胞激活。已知小胶质细胞具有修复和细胞毒性能力。在诸如缺血等急性损伤后已观察到神经元凋亡。小胶质细胞可能参与此过程。我们之前表明,从腹腔巨噬细胞或活化的小胶质细胞收集的条件培养基(CM)可触发培养的大鼠海马神经元凋亡。我们希望鉴定负责触发神经元死亡的因子。静止的小胶质细胞产生的CM不会破坏海马神经元。脂多糖激活的小胶质细胞产生的CM导致神经元死亡。纤溶酶原激活物抑制剂-1、tPA STOP以及与tPA抗体共同孵育可阻断这种效应。重组人tPA会加剧小胶质细胞CM的神经毒性作用,而单独的tPA仅在非常高的浓度下才具有毒性。这个体外系统可能排除了小胶质细胞自由基的任何显著影响,表明小胶质细胞tPA可能对海马神经元死亡有显著贡献。