Pitts Kristen M, Margeta Milica A
Department of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, MA, United States.
Schepens Eye Research Institute of Mass, Eye and Ear, Boston, MA, United States.
Front Cell Neurosci. 2023 Jan 26;17:1106547. doi: 10.3389/fncel.2023.1106547. eCollection 2023.
Microglia are dynamic guardians of neural tissue and the resident immune cells of the central nervous system (CNS). The disease-associated microglial signature (DAM), also known as the microglial neurodegenerative phenotype (MGnD), has gained significant attention in recent years as a fundamental microglial response common to various neurodegenerative disease pathologies. Interestingly, this signature shares many features in common with developmental microglia, suggesting the existence of recycled gene programs which play a role both in early neural circuit formation as well as in response to aging and disease. In addition, recent advances in single cell RNA sequencing have revealed significant heterogeneity within the original DAM signature, with contributions from both yolk sac-derived microglia as well as bone marrow-derived macrophages. In this review, we examine the role of the DAM signature in retinal development and disease, highlighting crosstalk between resident microglia and infiltrating monocytes which may critically contribute to the underlying mechanisms of age-related neurodegeneration.
小胶质细胞是神经组织的动态守护者以及中枢神经系统(CNS)的常驻免疫细胞。疾病相关小胶质细胞特征(DAM),也被称为小胶质细胞神经退行性表型(MGnD),近年来作为各种神经退行性疾病病理学中常见的一种基本小胶质细胞反应而备受关注。有趣的是,这种特征与发育中的小胶质细胞有许多共同特征,这表明存在循环利用的基因程序,其在早期神经回路形成以及对衰老和疾病的反应中均发挥作用。此外,单细胞RNA测序的最新进展揭示了原始DAM特征内存在显著的异质性,其中既有卵黄囊来源的小胶质细胞,也有骨髓来源的巨噬细胞的贡献。在这篇综述中,我们研究了DAM特征在视网膜发育和疾病中的作用,强调了常驻小胶质细胞和浸润单核细胞之间的相互作用,这可能对年龄相关性神经退行性变的潜在机制起关键作用。