Department of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Department of Pharmacology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Cells. 2022 Jun 22;11(13):2002. doi: 10.3390/cells11132002.
The miR-146 family consists of two microRNAs (miRNAs), miR-146a and miR-146b, which are both known to suppress a variety of immune responses. Here in this study, we show that miR-146b is abundantly expressed in neuronal cells, while miR-146a is mainly expressed in microglia and astroglia of adult mice. Accordingly, miR-146b deficient (-/-) mice exhibited anxiety-like behaviors and enhanced cognition. Characterization of cellular composition of -/- mice using flow cytometry revealed an increased number of neurons and a decreased abundancy of astroglia in the hippocampus and frontal cortex, whereas microglia abundancy remained unchanged. Immunohistochemistry showed a higher density of neurons in the frontal cortex of -/- mice, enhanced hippocampal neurogenesis as evidenced by an increased proliferation, and survival of newly generated cells with enhanced maturation into neuronal phenotype. No microglial activation or signs of neuroinflammation were observed in -/- mice. Further analysis demonstrated that miR-146b deficiency is associated with elevated expression of glial cell line-derived neurotrophic factor () mRNA in the hippocampus, which might be at least in part responsible for the observed neuronal expansion and the behavioral phenotype. This hypothesis is partially supported by the positive correlation between performance of mice in the object recognition test and mRNA expression in -/- mice. Together, these results show the distinct function of miR-146b in controlling behaviors and provide new insights in understanding cell-specific function of miR-146b in the neuronal and astroglial organization of the mouse brain.
miR-146 家族由两个 microRNAs(miRNAs)组成,miR-146a 和 miR-146b,它们都被认为可以抑制多种免疫反应。在本研究中,我们表明 miR-146b 在神经元细胞中大量表达,而 miR-146a 主要在成年小鼠的小胶质细胞和星形胶质细胞中表达。因此,miR-146b 缺陷(-/-)小鼠表现出焦虑样行为和增强的认知能力。使用流式细胞术对-/-小鼠的细胞组成进行特征分析表明,海马体和额叶皮质中的神经元数量增加,星形胶质细胞数量减少,而小胶质细胞数量保持不变。免疫组织化学显示-/-小鼠额叶皮质中的神经元密度更高,海马体中的神经发生增强,表现为增殖增加,新生成的细胞存活并向神经元表型成熟。在-/-小鼠中未观察到小胶质细胞激活或神经炎症的迹象。进一步分析表明,miR-146b 缺陷与海马体中神经胶质细胞系衍生的神经营养因子()mRNA 的表达升高有关,这可能至少部分解释了观察到的神经元扩张和行为表型。这一假设部分得到了-/-小鼠在物体识别测试中的表现与 mRNA 表达之间存在正相关的支持。总之,这些结果表明 miR-146b 在控制行为方面具有独特的功能,并为理解 miR-146b 在小鼠大脑神经元和星形胶质细胞组织中的细胞特异性功能提供了新的见解。