Streit W J, Graeber M B, Kreutzberg G W
Department of Neuromorphology, Max Planck Institute of Psychiatry, Martinsried, Federal Republic of Germany.
Glia. 1988;1(5):301-7. doi: 10.1002/glia.440010502.
The present review summarizes recently acquired data in vivo, which support a role of CNS microglia as a source of defense cells in the CNS capable of carrying out certain immune functions autonomously. We have kept the following discussion restricted to microglial cells and have not included work on the immunological functions of astrocytes, which has been recently reviewed elsewhere (Fontana et al.: Immunological Reviews 137:3521-3527, 1987). Resting microglia are scattered uniformly throughout the CNS forming a network of potential immunoeffector cells, which can be activated by stimuli ranging from peripheral nerve injury over viral infections to direct mechanical brain trauma. The term "activated microglia" is used here to describe proliferating cells that demonstrate changes in their immunophenotype but have not undergone transformation into brain macrophages. Such a transformation can be stimulated by neuronal death but not by sublethal neuronal injury. Microglia may function as antigen-presenting cells and may thus represent the effector cell responsible for the recruitment of lymphocytes to the brain resulting in an inflammatory reaction. The recent developments in the understanding of microglial cell function may lead to a redefinition of the often cited "immune privilege" of the brain.
本综述总结了最近在体内获得的数据,这些数据支持中枢神经系统小胶质细胞作为中枢神经系统防御细胞来源的作用,能够自主执行某些免疫功能。我们将以下讨论限制在小胶质细胞,未纳入有关星形胶质细胞免疫功能的研究,该方面最近已有其他综述(丰塔纳等人:《免疫学综述》137:3521 - 3527,1987年)。静息小胶质细胞均匀地散布于整个中枢神经系统,形成一个潜在免疫效应细胞网络,可被从外周神经损伤、病毒感染到直接脑机械创伤等各种刺激激活。这里使用“活化小胶质细胞”一词来描述增殖细胞,这些细胞表现出免疫表型的变化,但尚未转变为脑巨噬细胞。这种转变可由神经元死亡刺激引发,但亚致死性神经元损伤则无法刺激其发生。小胶质细胞可能作为抗原呈递细胞,因此可能是负责将淋巴细胞募集到脑内从而引发炎症反应的效应细胞。对小胶质细胞功能理解的最新进展可能会导致对常被提及的脑“免疫特权”进行重新定义。