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Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures

机译:单细胞转录组学揭示了不同的炎症诱导的小胶质细胞信号

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摘要

Microglia are specialized parenchymal‐resident phagocytes of the central nervous system (CNS) that actively support, defend and modulate the neural environment. Dysfunctional microglial responses are thought to worsen CNS diseases; nevertheless, their impact during neuroinflammatory processes remains largely obscure. Here, using a combination of single‐cell RNA sequencing and multicolour flow cytometry, we comprehensively profile microglia in the brain of lipopolysaccharide (LPS)‐injected mice. By excluding the contribution of other immune CNS‐resident and peripheral cells, we show that microglia isolated from LPS‐injected mice display a global downregulation of their homeostatic signature together with an upregulation of inflammatory genes. Notably, we identify distinct microglial activated profiles under inflammatory conditions, which greatly differ from neurodegenerative disease‐associated profiles. These results provide insights into microglial heterogeneity and establish a resource for the identification of specific phenotypes in CNS disorders, such as neuroinflammatory and neurodegenerative diseases.
机译:小胶质细胞是中枢神经系统(CNS)的专门的实质性吞噬细胞,可主动支持,防御和调节神经环境。小胶质细胞功能障碍的反应被认为使中枢神经系统疾病恶化。然而,它们在神经发炎过程中的影响仍然不清楚。在这里,结合使用单细胞RNA测序和多色流式细胞术,我们对注射脂多糖(LPS)的小鼠大脑中的小胶质细胞进行了全面分析。通过排除其他免疫中枢神经系统驻留和外周细胞的贡献,我们表明,从注射LPS的小鼠中分离出的小胶质细胞显示出其体内稳态标记的整体下调以及炎性基因的上调。值得注意的是,我们在炎性条件下识别出不同的小神经胶质激活特征,这与神经退行性疾病相关特征大不相同。这些结果提供了对小胶质细胞异质性的见识,并为鉴定中枢神经系统疾病(例如神经炎性疾病和神经退行性疾病)中的特定表型提供了资源。

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