Dermitzakis Iasonas, Manthou Maria Eleni, Meditskou Soultana, Tremblay Marie-Ève, Petratos Steven, Zoupi Lida, Boziki Marina, Kesidou Evangelia, Simeonidou Constantina, Theotokis Paschalis
Department of Histology-Embryology, School of Medicine, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Division of Medical Sciences, University of Victoria, Victoria, BC V8P 5C2, Canada.
Curr Issues Mol Biol. 2023 Mar 22;45(3):2609-2628. doi: 10.3390/cimb45030171.
Microglia belong to tissue-resident macrophages of the central nervous system (CNS), representing the primary innate immune cells. This cell type constitutes ~7% of non-neuronal cells in the mammalian brain and has a variety of biological roles integral to homeostasis and pathophysiology from the late embryonic to adult brain. Its unique identity that distinguishes its "glial" features from tissue-resident macrophages resides in the fact that once entering the CNS, it is perennially exposed to a unique environment following the formation of the blood-brain barrier. Additionally, tissue-resident macrophage progenies derive from various peripheral sites that exhibit hematopoietic potential, and this has resulted in interpretation issues surrounding their origin. Intensive research endeavors have intended to track microglial progenitors during development and disease. The current review provides a corpus of recent evidence in an attempt to disentangle the birthplace of microglia from the progenitor state and underlies the molecular elements that drive microgliogenesis. Furthermore, it caters towards tracking the lineage spatiotemporally during embryonic development and outlining microglial repopulation in the mature CNS. This collection of data can potentially shed light on the therapeutic potential of microglia for CNS perturbations across various levels of severity.
小胶质细胞属于中枢神经系统(CNS)的组织驻留巨噬细胞,是主要的固有免疫细胞。这种细胞类型占哺乳动物大脑中非神经元细胞的约7%,从胚胎后期到成年大脑,它在维持内环境稳定和病理生理学方面具有多种重要的生物学作用。其将“胶质”特征与组织驻留巨噬细胞区分开来的独特身份在于,一旦进入中枢神经系统,在血脑屏障形成后,它就会长期暴露于独特的环境中。此外,组织驻留巨噬细胞后代源自具有造血潜能的各种外周部位,这导致了围绕其起源的解释问题。大量研究致力于追踪发育和疾病过程中的小胶质细胞祖细胞。本综述提供了一系列最新证据,试图厘清小胶质细胞从祖细胞状态开始的起源地,并揭示驱动小胶质细胞生成的分子因素。此外,它有助于在胚胎发育过程中时空追踪谱系,并概述成熟中枢神经系统中小胶质细胞的重新填充。这些数据收集可能为不同严重程度的中枢神经系统紊乱中小胶质细胞的治疗潜力提供线索。