Department of Neurobiology Research, Institute for Molecular Medicine, University of Southern Denmark, Odense, Denmark.
BRIDGE, Brain Research - Inter-Disciplinary Guided Excellence, Odense, Denmark.
Front Immunol. 2020 Apr 3;11:430. doi: 10.3389/fimmu.2020.00430. eCollection 2020.
Microglial heterogeneity has been the topic of much discussion in the scientific community. Elucidation of their plasticity and adaptability to disease states triggered early efforts to characterize microglial subsets. Over time, their phenotypes, and later on their homeostatic signature, were revealed, through the use of increasingly advanced transcriptomic techniques. Recently, an increasing number of these "microglial signatures" have been reported in various homeostatic and disease contexts. Remarkably, many of these states show similar overlapping microglial gene expression patterns, both in homeostasis and in disease or injury. In this review, we integrate information from these studies, and we propose a unique subset, for which we introduce a core signature, based on our own research and reports from the literature. We describe that this subset is found in development and in normal aging as well as in diverse diseases. We discuss the functions of this subset as well as how it is induced.
小胶质细胞的异质性一直是科学界讨论的主题。阐明它们对疾病状态的可塑性和适应性促使人们早期努力对小胶质细胞亚群进行特征描述。随着时间的推移,通过使用越来越先进的转录组学技术,揭示了它们的表型,后来又揭示了它们的稳态特征。最近,在各种稳态和疾病背景下,越来越多的这些“小胶质细胞特征”被报道。值得注意的是,许多这些状态在稳态和疾病或损伤中都显示出相似的重叠小胶质细胞基因表达模式。在这篇综述中,我们整合了这些研究的信息,并根据我们自己的研究和文献报告,提出了一个独特的亚群,并为其引入了一个核心特征。我们描述了这个亚群存在于发育和正常衰老中,以及在各种疾病中。我们讨论了这个亚群的功能以及它是如何被诱导的。