Institute of Neuropathology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
BIOSS Centre for Biological Signalling Studies, University of Freiburg, Freiburg, Germany.
Nat Immunol. 2017 Mar 22;18(4):385-392. doi: 10.1038/ni.3703.
Myeloid cells in the central nervous system (CNS) represent a heterogeneous class of innate immune cells that contribute to the maintenance of tissue homeostasis differentially during development and adulthood. The subsets of CNS myeloid cells identified so far, including parenchymal microglia and non-parenchymal meningeal, perivascular and choroid-plexus macrophages, as well as disease-associated monocytes, have classically been distinguished on the basis of their surface epitope expression, localization and morphology. However, studies using cell-specific targeting, in vivo imaging, single-cell expression analysis and other sophisticated tools have now increased the depth of knowledge of this immune-cell compartment and call for reevaluation of the traditional views on the origin, fate and function of distinct CNS myeloid subsets. The concepts of CNS macrophage biology that are emerging from these new insights have broad implications for the understanding and treatment of CNS diseases.
中枢神经系统 (CNS) 中的髓样细胞是一类异质性的固有免疫细胞,它们在发育和成年期对组织稳态的维持有不同的作用。迄今为止鉴定的 CNS 髓样细胞亚群,包括实质小胶质细胞和非实质脑膜、血管周和脉络丛巨噬细胞,以及与疾病相关的单核细胞,其表面表位表达、定位和形态特征一直是区分它们的依据。然而,使用细胞特异性靶向、体内成像、单细胞表达分析和其他复杂工具的研究,现在已经加深了对这个免疫细胞区室的了解,并需要重新评估传统的关于不同 CNS 髓样细胞亚群的起源、命运和功能的观点。这些新的见解所带来的中枢神经系统巨噬细胞生物学概念,对中枢神经系统疾病的理解和治疗具有广泛的意义。