Department of Neurology, Ruijin Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200025, China; Neuroscience and Neuroengineering Research Center, Med-X Research Institute and School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai 200030, China.
Neuroscience and Neuroengineering Research Center, Med-X Research Institute and School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai 200030, China; Department of Rehabilitation, Ruijin Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200025, China.
Prog Neurobiol. 2017 Oct;157:247-272. doi: 10.1016/j.pneurobio.2016.01.005. Epub 2016 Feb 2.
Microglia are brain resident macrophages originated from primitive progenitor cells in the yolk sac. Microglia can be activated within hours and recruited to the lesion site. Traditionally, microglia activation is considered to play a deleterious role in ischemic stroke, as inhibition of microglia activation attenuates ischemia induced brain injury. However, increasing evidence show that microglia activation is critical for attenuating neuronal apoptosis, enhancing neurogenesis, and promoting functional recovery after cerebral ischemia. Differential polarization of microglia could likely explain the biphasic role of microglia in ischemia. We comprehensively reviewed the mechanisms involved in regulating microglia activation and polarization. The latest discoveries of microRNAs in modulating microglia function are discussed. In addition, the interaction between microglia and other cells including neurons, astrocytes, oligodendrocytes, and stem cells were also reviewed. Future therapies targeting microglia may not exclusively aim at suppressing microglia activation, but also at modulating microglia polarization at different stages of ischemic stroke. More work is needed to elucidate the cellular and molecular mechanisms of microglia polarization under ischemic environment. The roles of microRNAs and transplanted stem cells in mediating microglia activation and polarization during brain ischemia also need to be further studied.
小胶质细胞是大脑驻留巨噬细胞,起源于卵黄囊中的原始祖细胞。小胶质细胞可以在数小时内被激活,并募集到损伤部位。传统上,小胶质细胞的激活被认为在缺血性中风中起有害作用,因为抑制小胶质细胞的激活可以减轻缺血引起的脑损伤。然而,越来越多的证据表明,小胶质细胞的激活对于减轻神经元凋亡、增强神经发生和促进脑缺血后的功能恢复至关重要。小胶质细胞的差异极化可能可以解释小胶质细胞在缺血中的双相作用。我们全面回顾了调节小胶质细胞激活和极化的机制。讨论了 microRNAs 在调节小胶质细胞功能方面的最新发现。此外,还综述了小胶质细胞与神经元、星形胶质细胞、少突胶质细胞和干细胞等其他细胞之间的相互作用。未来针对小胶质细胞的治疗方法可能不仅要抑制小胶质细胞的激活,还要在缺血性中风的不同阶段调节小胶质细胞的极化。需要进一步阐明在缺血环境中小胶质细胞极化的细胞和分子机制。还需要进一步研究 microRNAs 和移植的干细胞在介导脑缺血中小胶质细胞激活和极化中的作用。