Institute of Neuroscience and Key Laboratory of Molecular Neurobiology of the Ministry of Education, Neuroscience Research Center of Changzheng Hospital, Second Military Medical University, Shanghai 200433, China.
Neurosci Bull. 2013 Apr;29(2):189-98. doi: 10.1007/s12264-013-1324-0. Epub 2013 Apr 5.
Multiple sclerosis (MS) is an autoimmune demyelinating disease of the central nervous system, and microglia and macrophages play important roles in its pathogenesis. The activation of microglia and macrophages accompanies disease development, whereas depletion of these cells significantly decreases disease severity. Microglia and macrophages usually have diverse and plastic phenotypes. Both pro-inflammatory and antiinflammatory microglia and macrophages exist in MS and its animal model, experimental autoimmune encephalomyelitis. The polarization of microglia and macrophages may underlie the differing functional properties that have been reported. in this review, we discuss the responses and polarization of microglia and macrophages in MS, and their effects on its pathogenesis and repair. Harnessing their beneficial effects by modulating their polarization states holds great promise for the treatment of inflammatory demyelinating diseases.
多发性硬化症(MS)是一种中枢神经系统自身免疫性脱髓鞘疾病,小胶质细胞和巨噬细胞在其发病机制中起重要作用。小胶质细胞和巨噬细胞的激活伴随着疾病的发展,而这些细胞的耗竭则显著降低疾病的严重程度。小胶质细胞和巨噬细胞通常具有多样化和可塑的表型。在 MS 及其动物模型实验性自身免疫性脑脊髓炎中存在促炎和抗炎的小胶质细胞和巨噬细胞。小胶质细胞和巨噬细胞的极化可能是导致其报道的不同功能特性的基础。在这篇综述中,我们讨论了 MS 中小胶质细胞和巨噬细胞的反应和极化及其对发病机制和修复的影响。通过调节其极化状态利用它们的有益作用,为治疗炎症性脱髓鞘疾病带来了巨大的希望。