Bridlance Cécile, Thion Morgane Sonia
Institut de Biologie de l'École Normale Supérieure (IBENS), École Normale Supérieure, CNRS, INSERM, Université PSL, Paris, France.
Center for Interdisciplinary Research in Biology, Collège de France, CNRS, INSERM, Université PSL, Paris, France.
Front Neurosci. 2023 Mar 23;17:1125729. doi: 10.3389/fnins.2023.1125729. eCollection 2023.
Microglia, the brain resident macrophages, are multifaceted glial cells that belong to the central nervous and immune systems. As part of the immune system, they mediate innate immune responses, regulate brain homeostasis and protect the brain in response to inflammation or injury. At the same time, they can perform a wide array of cellular functions that relate to the normal functioning of the brain. Importantly, microglia are key actors of brain development. Indeed, these early brain invaders originate outside of the central nervous system from yolk sac myeloid progenitors, and migrate into the neural folds during early embryogenesis. Before the generation of oligodendrocytes and astrocytes, microglia thus occupy a unique position, constituting the main glial population during early development and participating in a wide array of embryonic and postnatal processes. During this developmental time window, microglia display remarkable features, being highly heterogeneous in time, space, morphology and transcriptional states. Although tremendous progress has been made in our understanding of their ontogeny and roles, there are several limitations for the investigation of specific microglial functions as well as their heterogeneity during development. This review summarizes the current murine tools and models used in the field to study the development of these peculiar cells. In particular, we focus on the methodologies used to label and deplete microglia, monitor their behavior through live-imaging and also discuss the progress currently being made by the community to unravel microglial functions in brain development and disorders.
小胶质细胞是脑内常驻巨噬细胞,是属于中枢神经系统和免疫系统的多面性神经胶质细胞。作为免疫系统的一部分,它们介导先天性免疫反应,调节脑内稳态,并在炎症或损伤时保护大脑。同时,它们可以执行与大脑正常功能相关的一系列细胞功能。重要的是,小胶质细胞是脑发育的关键参与者。实际上,这些早期侵入大脑的细胞起源于中枢神经系统之外的卵黄囊髓系祖细胞,并在胚胎早期发育过程中迁移到神经褶中。在少突胶质细胞和星形胶质细胞产生之前,小胶质细胞因此占据着独特的位置,在早期发育过程中构成主要的神经胶质群体,并参与一系列胚胎和出生后的过程。在这个发育时间窗口内,小胶质细胞表现出显著的特征,在时间、空间、形态和转录状态上具有高度的异质性。尽管我们对它们的个体发生和作用的理解取得了巨大进展,但在研究特定小胶质细胞功能及其在发育过程中的异质性方面仍存在一些局限性。本综述总结了该领域目前用于研究这些特殊细胞发育的小鼠工具和模型。特别是,我们重点关注用于标记和清除小胶质细胞、通过活体成像监测其行为的方法,并讨论了该领域目前在揭示小胶质细胞在脑发育和疾病中的功能方面所取得的进展。