Department of Molecular Microbiology & Immunology, The University of Texas at San Antonio, San Antonio, TX, USA.
South Texas Center for Emerging Infectious Diseases, The University of Texas at San Antonio, San Antonio, TX, USA.
Adv Neurobiol. 2024;37:263-286. doi: 10.1007/978-3-031-55529-9_15.
Microglia are best known as the resident phagocytes of the central nervous system (CNS). As a resident brain immune cell population, microglia play key roles during the initiation, propagation, and resolution of inflammation. The discovery of resident adaptive immune cells in the CNS has unveiled a relationship between microglia and adaptive immune cells for CNS immune-surveillance during health and disease. The interaction of microglia with elements of the peripheral immune system and other CNS resident cells mediates a fine balance between neuroprotection and tissue damage. In this chapter, we highlight the innate immune properties of microglia, with a focus on how pattern recognition receptors, inflammatory signaling cascades, phagocytosis, and the interaction between microglia and adaptive immune cells regulate events that initiate an inflammatory or neuroprotective response within the CNS that modulates immune-mediated disease exacerbation or resolution.
小胶质细胞作为中枢神经系统(CNS)的固有吞噬细胞而广为人知。作为驻留脑免疫细胞群体,小胶质细胞在炎症的启动、传播和消退中发挥关键作用。在中枢神经系统中发现常驻适应性免疫细胞,揭示了小胶质细胞与适应性免疫细胞之间的关系,有助于中枢神经系统在健康和疾病期间进行免疫监视。小胶质细胞与外周免疫系统和其他中枢神经系统驻留细胞的相互作用,介导了神经保护和组织损伤之间的精细平衡。在本章中,我们强调了小胶质细胞的固有免疫特性,重点介绍了模式识别受体、炎症信号级联、吞噬作用以及小胶质细胞与适应性免疫细胞的相互作用如何调节中枢神经系统内启动炎症或神经保护反应的事件,从而调节免疫介导的疾病恶化或缓解。