Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States.
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States.
Adv Immunol. 2018;139:1-50. doi: 10.1016/bs.ai.2018.04.002. Epub 2018 May 9.
Microglia are a subset of tissue macrophages that constitute the major immune cell type of the central nervous system. These cells have long been known to change their morphology and functions in response to various neurological insults. Recently, a plethora of unbiased transcriptomics studies have revealed that across a broad spectrum of neurodegeneration-like disease models, microglia adopt a similar activation signature and perform similar functions. Despite these commonalities in response, the role of microglia has been described as both positive and negative in different murine disease models. In humans, genetic association studies have revealed strong connections between microglia genes and various neurodegenerative diseases, and mechanistic investigations of these mutations have added another layer of complexity. Here, we provide an overview of studies that have built a case for a common microglial response to neurodegeneration and discuss pathways that may be important to initiate and sustain this response; delineate the multifaceted functions of activated microglia spanning different diseases; and discuss insights from studying genes associated with disease in humans. We argue that strong evidence causally links activated microglia function to neurodegeneration and discuss what seems to be a conflict between mouse models and human genetics.
小胶质细胞是组织巨噬细胞的一个子集,构成了中枢神经系统的主要免疫细胞类型。这些细胞的形态和功能在应对各种神经损伤时会发生变化,这一点早已为人所知。最近,大量无偏倚的转录组学研究表明,在广泛的神经退行性疾病模型中,小胶质细胞表现出相似的激活特征并发挥相似的功能。尽管在反应上存在这些共性,但小胶质细胞在不同的小鼠疾病模型中的作用被描述为既有积极的也有消极的。在人类中,遗传关联研究揭示了小胶质细胞基因与各种神经退行性疾病之间的强烈关联,对这些突变的机制研究又增加了一层复杂性。在这里,我们提供了对支持神经退行性变中小胶质细胞共同反应的研究的概述,并讨论了可能对启动和维持这种反应很重要的途径;描述了激活的小胶质细胞在不同疾病中的多方面功能;并讨论了从研究与人类疾病相关的基因中获得的见解。我们认为,激活的小胶质细胞功能与神经退行性变之间存在因果关系的有力证据,并讨论了小鼠模型和人类遗传学之间似乎存在的冲突。