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微小RNA-9通过靶向MCPIP1促进小胶质细胞活化。

MiR-9 promotes microglial activation by targeting MCPIP1.

作者信息

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

机构信息

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].

出版信息

Nat Commun. 2014 Jul 14;5:4386. doi: 10.1038/ncomms5386.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0572/4104446/712ff8de50ac/ncomms5386-f1.jpg

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