Yao Honghong, Ma Rong, Yang Lu, Hu Guoku, Chen Xufeng, Duan Ming, Kook Yeonhee, Niu Fang, Liao Ke, Fu Minggui, Hu Gang, Kolattukudy Pappachan, Buch Shilpa
1] Department of Pharmacology, Medical School of Southeast University, Nanjing, Jiangsu 210009, China [2].
1] Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, Nebraska 68198-5880, USA [2].
Nat Commun. 2014 Jul 14;5:4386. doi: 10.1038/ncomms5386.
Microglia participate in innate inflammatory responses within the central nervous system. The highly conserved microRNA-9 (miR-9) plays critical roles in neurogenesis as well as axonal extension. Its role in microglial inflammatory responses, however, remains poorly understood. Here we identify a unique role of miR-9 in mediating the microglial inflammatory response via distinct signalling pathways. MiR-9-mediated regulation of cellular activation involved downregulated expression of the target protein, monocyte chemotactic protein-induced protein 1 (MCPIP1) that is crucial for controlling inflammation. Results indicate that miR-9-mediated cellular activation involved signalling via the NF-κB pathway, but not the β-catenin pathway.
小胶质细胞参与中枢神经系统内的先天性炎症反应。高度保守的微小RNA-9(miR-9)在神经发生以及轴突延伸中起关键作用。然而,其在小胶质细胞炎症反应中的作用仍知之甚少。在这里,我们确定了miR-9在通过不同信号通路介导小胶质细胞炎症反应中的独特作用。miR-9介导的细胞活化调节涉及靶蛋白单核细胞趋化蛋白诱导蛋白1(MCPIP1)表达下调,而该蛋白对控制炎症至关重要。结果表明,miR-9介导的细胞活化涉及通过NF-κB途径而非β-连环蛋白途径的信号传导。