Institute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
Institute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
Neuron. 2022 Nov 2;110(21):3497-3512. doi: 10.1016/j.neuron.2022.10.005.
CNS-resident macrophages-including parenchymal microglia and border-associated macrophages (BAMs)-contribute to neuronal development and health, vascularization, and tissue integrity at steady state. Border-patrolling mononuclear phagocytes such as dendritic cells and monocytes confer important immune functions to the CNS, protecting it from pathogenic threats including aberrant cell growth and brain malignancies. Even though we have learned much about the contribution of lymphocytes to CNS pathologies, a better understanding of differential roles of tissue-resident and -invading phagocytes is slowly emerging. In this perspective, we propose that in CNS neuroinflammatory diseases, tissue-resident macrophages (TRMs) contribute to the clearing of debris and resolution of inflammation, whereas blood-borne phagocytes are drivers of immunopathology. We discuss the remaining challenges to resolve which specialized mononuclear phagocyte populations are driving or suppressing immune effector function, thereby potentially dictating the outcome of autoimmunity or brain cancer.
中枢神经系统驻留巨噬细胞,包括实质小胶质细胞和边缘相关巨噬细胞(BAMs),在稳态下有助于神经元发育和健康、血管生成和组织完整性。边界巡逻的单核吞噬细胞,如树突状细胞和单核细胞,为中枢神经系统赋予了重要的免疫功能,使其免受包括异常细胞生长和脑恶性肿瘤在内的致病威胁。尽管我们已经了解了淋巴细胞对中枢神经系统疾病的贡献,但对于组织驻留和浸润性吞噬细胞的不同作用的理解正在缓慢出现。在这方面,我们提出,在中枢神经系统神经炎症性疾病中,组织驻留巨噬细胞(TRMs)有助于清除碎片和炎症消退,而血源性吞噬细胞是免疫病理的驱动因素。我们讨论了仍然存在的挑战,以确定哪些特化的单核吞噬细胞群体正在驱动或抑制免疫效应功能,从而可能决定自身免疫或脑癌的结果。