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Dicer 缺陷对发育中和成年期大脑的小胶质细胞有差异影响。

Dicer Deficiency Differentially Impacts Microglia of the Developing and Adult Brain.

机构信息

Department of Immunology, The Weizmann Institute of Science, 76100 Rehovot, Israel.

Institute of Neuropathology, Medical Faculty, University of Freiburg, 79106 Freiburg, Germany.

出版信息

Immunity. 2017 Jun 20;46(6):1030-1044.e8. doi: 10.1016/j.immuni.2017.05.003.

Abstract

Microglia seed the embryonic neuro-epithelium, expand and actively sculpt neuronal circuits in the developing central nervous system, but eventually adopt relative quiescence and ramified morphology in the adult. Here, we probed the impact of post-transcriptional control by microRNAs (miRNAs) on microglial performance during development and adulthood by generating mice lacking microglial Dicer expression at these distinct stages. Conditional Dicer ablation in adult microglia revealed that miRNAs were required to limit microglial responses to challenge. After peripheral endotoxin exposure, Dicer-deficient microglia expressed more pro-inflammatory cytokines than wild-type microglia and thereby compromised hippocampal neuronal functions. In contrast, prenatal Dicer ablation resulted in spontaneous microglia activation and revealed a role for Dicer in DNA repair and preservation of genome integrity. Accordingly, Dicer deficiency rendered otherwise radio-resistant microglia sensitive to gamma irradiation. Collectively, the differential impact of the Dicer ablation on microglia of the developing and adult brain highlights the changes these cells undergo with time.

摘要

小胶质细胞为胚胎神经上皮细胞的种子细胞,在中枢神经系统的发育过程中扩增并积极塑造神经元回路,但最终在成年后会进入相对静止和分支形态。在这里,我们通过生成在这些不同阶段缺乏小胶质细胞 Dicer 表达的小鼠,探究了 microRNAs (miRNAs) 对小胶质细胞发育和成年期表现的转录后控制的影响。在成年小胶质细胞中条件性 Dicer 缺失表明,miRNAs 对于限制小胶质细胞对挑战的反应是必需的。在外周内毒素暴露后,与野生型小胶质细胞相比,Dicer 缺陷型小胶质细胞表达了更多的促炎细胞因子,从而损害了海马神经元功能。相比之下,产前 Dicer 缺失导致小胶质细胞自发激活,并揭示了 Dicer 在 DNA 修复和基因组完整性维持中的作用。因此,Dicer 缺陷使本来对伽马辐射有抗性的小胶质细胞对其敏感。总的来说,Dicer 缺失对发育中和成年期大脑中小胶质细胞的不同影响突出了这些细胞随时间发生的变化。

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