Schiefer J, Töpper R, Schmidt W, Block F, Heinrich P C, Noth J, Schwarz M
Department of Neurology, Technical University Aachen, Germany.
J Neuroimmunol. 1998 Aug 14;89(1-2):168-76. doi: 10.1016/s0165-5728(98)00133-7.
Stereotaxic intrastriatal injection of the naturally occurring N-methyl-D-aspartate (NMDA) agonist quinolinic acid (QA) serves as a valuable in vivo model to study excitotoxic cell damage in the central nervous system (CNS). Although morphological changes such as neuronal loss, glial activation and remote reactions following QA injection have been described in some detail, much less is known about the molecular mechanisms mediating the accompanying glial response. Cytokines are known to play a crucial role in almost all kinds of CNS alterations. We now demonstrate that IL-6, a multifunctional glycoprotein which belongs to the family of neurokines, is expressed endogenously in the rat striatum following QA injection. Using Northern blot analysis, a massive but transient upregulation of IL-6 mRNA could be detected. This started 3 h after QA injection, reached a maximum at 6 h and disappeared within 24 h. That activated microglia are the most likely cellular source of the observed corresponding IL-6 protein expression could be concluded by comparing the immunocytochemical pattern of IL-6 expression and microglial activation. Interestingly, astrocytes initially downregulate their expression of glial fibrillary acidic protein (GFAP) in the excitotoxically injured striatum, but show a delayed increase in GFAP immunoreactivity starting in the periphery of the striatum, subsequently expanding to the core. The early transient IL-6 expression may play an important role in initiating the delayed astrocytic response following excitotoxic cell injury.
立体定向向纹状体内注射天然存在的N-甲基-D-天冬氨酸(NMDA)激动剂喹啉酸(QA),是研究中枢神经系统(CNS)兴奋性毒性细胞损伤的一种有价值的体内模型。尽管QA注射后诸如神经元丢失、胶质细胞活化和远隔反应等形态学变化已得到较为详细的描述,但对于介导伴随的胶质细胞反应的分子机制却知之甚少。已知细胞因子在几乎所有类型的CNS改变中都起着关键作用。我们现在证明,IL-6作为一种属于神经因子家族的多功能糖蛋白,在QA注射后在大鼠纹状体内内源性表达。通过Northern印迹分析,可检测到IL-6 mRNA大量但短暂地上调。这在QA注射后3小时开始,在6小时达到峰值,并在24小时内消失。通过比较IL-6表达的免疫细胞化学模式和小胶质细胞活化情况,可以得出活化的小胶质细胞是观察到的相应IL-6蛋白表达最可能的细胞来源这一结论。有趣的是,星形胶质细胞最初在兴奋性毒性损伤的纹状体内下调其胶质纤维酸性蛋白(GFAP)的表达,但在纹状体周边开始显示GFAP免疫反应性延迟增加,随后扩展至核心区域。早期短暂的IL-6表达可能在兴奋性毒性细胞损伤后引发延迟的星形胶质细胞反应中起重要作用。