Department of Functional Anatomy and Neuroscience, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Department of Genetics, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.
EMBO J. 2020 Nov 16;39(22):e104464. doi: 10.15252/embj.2020104464. Epub 2020 Sep 22.
Microglia are the principal phagocytes that clear cell debris in the central nervous system (CNS). This raises the question, which cells remove cell debris when microglial phagocytic activity is impaired. We addressed this question using Siglech mice, which enable highly specific ablation of microglia. Non-microglial mononuclear phagocytes, such as CNS-associated macrophages and circulating inflammatory monocytes, did not clear microglial debris. Instead, astrocytes were activated, exhibited a pro-inflammatory gene expression profile, and extended their processes to engulf microglial debris. This astrocytic phagocytosis was also observed in Irf8-deficient mice, in which microglia were present but dysfunctional. RNA-seq demonstrated that even in a healthy CNS, astrocytes express TAM phagocytic receptors, which were the main astrocytic phagocytic receptors for cell debris in the above experiments, indicating that astrocytes stand by in case of microglial impairment. This compensatory mechanism may be important for the maintenance or prolongation of a healthy CNS.
小胶质细胞是清除中枢神经系统 (CNS) 细胞碎片的主要吞噬细胞。这就提出了一个问题,当小胶质细胞吞噬活性受损时,哪些细胞会清除细胞碎片。我们使用 Siglech 小鼠来解决这个问题,Siglech 小鼠能够高度特异性地清除小胶质细胞。非小胶质细胞单核吞噬细胞,如中枢神经系统相关巨噬细胞和循环炎症性单核细胞,不能清除小胶质细胞碎片。相反,星形胶质细胞被激活,表现出促炎基因表达谱,并延伸其过程以吞噬小胶质细胞碎片。这种星形胶质细胞吞噬作用也在 Irf8 缺陷小鼠中观察到,其中小胶质细胞存在但功能失调。RNA-seq 表明,即使在健康的中枢神经系统中,星形胶质细胞也表达 TAM 吞噬受体,这些受体是上述实验中小胶质细胞碎片的主要星形胶质细胞吞噬受体,表明星形胶质细胞在小胶质细胞损伤时待命。这种代偿机制对于维持或延长健康的中枢神经系统可能很重要。