| Literature DB >> 25962782 |
Yong Zhang1, Mingfeng Guo2, Ning Xin3, Zhen Shao4, Xiuying Zhang4, Yanyan Zhang4, Jing Chen4, Shuangshuang Zheng4, Linlin Fu5, YuZhong Wang6, Dongmei Zhou5, Hao Chen4, Yan Huang4, Ruiguo Dong7, Chenghua Xiao4, Yonghai Liu4, Deqin Geng4.
Abstract
miR-181c is a newly identified negative regulator of immune cell activation. In this study, we aimed to investigate the expression and functional role of miR-181c in myasthenia gravis (MG). miR-181c showed significant downregulation in peripheral blood mononuclear cells (PBMCs) from MG patients compared with healthy controls, with lower expression in generalized patients than in ocular ones. MG patients also had increased serum IL-7 and IL-17 levels. Additionally, serum IL-7 level presents a positive correlation with the serum IL-17 level. miR-181c levels were negatively correlated with serum levels of IL-7 and IL-17 in either generalized patients or ocular patients. A luciferase reporter assay revealed that miR-181c could directly bind to the 3'-UTR of interleukin-7. Forced expression of miR-181c led to decreased IL-7 and IL-17 release in cultured PBMCs, while depletion of miR-181c increased the secretion of these two proinflammatory cytokines. The results from our study suggested for the first time that miR-181c was able to negatively regulate the production of proinflammatory cytokines IL-7 and IL-17 in MG patients, and it is a novel potential therapeutic target for MG.Entities:
Keywords: IL-17; IL-7; MiR-181c; MicroRNAs; Myasthenia gravis
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Year: 2015 PMID: 25962782 DOI: 10.1007/s10238-015-0358-1
Source DB: PubMed Journal: Clin Exp Med ISSN: 1591-8890 Impact factor: 3.984