Carson Monica J
Department of Molecular Biology, Scripps Research Institute, La Jolla, California.
Glia. 2002 Nov;40(2):218-231. doi: 10.1002/glia.10145.
Multiple sclerosis is a chronic demyelinating inflammatory disease of the central nervous system (CNS). As the tissue macrophage of the CNS, microglia have the potential to regulate and be regulated by cells of the CNS and by CNS-infiltrating immune cells. The exquisite sensitivity of microglia to these signals, coupled with their ability to develop a broad range of effector functions, allows the CNS to tailor microglial function for specific physiological needs. However, the great plasticity of microglial responses can also predispose these cells to amplify disproportionately the irrelevant or dysfunctional signals provided by either the CNS or immune systems. The consequences of such an event could be the conversion of self-limiting inflammatory responses into chronic neurodegeneration and may explain in part the heterogeneous nature of multiple sclerosis.
多发性硬化症是一种中枢神经系统(CNS)的慢性脱髓鞘炎症性疾病。作为中枢神经系统的组织巨噬细胞,小胶质细胞有潜力被中枢神经系统细胞以及浸润中枢神经系统的免疫细胞调节,并对它们进行调节。小胶质细胞对这些信号的高度敏感性,加上它们产生广泛效应功能的能力,使中枢神经系统能够根据特定的生理需求调整小胶质细胞的功能。然而,小胶质细胞反应的高度可塑性也可能使这些细胞过度放大由中枢神经系统或免疫系统提供的不相关或功能失调的信号。这种情况的后果可能是将自限性炎症反应转化为慢性神经退行性变,这可能部分解释了多发性硬化症的异质性。