Decreased microRNA miR-181c expression in peripheral blood mononuclear cells correlates with elevated serum levels of IL-7 and IL-17 in patients with myasthenia gravis

被引:0
作者
Yong Zhang
Mingfeng Guo
Ning Xin
Zhen Shao
Xiuying Zhang
Yanyan Zhang
Jing Chen
Shuangshuang Zheng
Linlin Fu
YuZhong Wang
Dongmei Zhou
Hao Chen
Yan Huang
Ruiguo Dong
Chenghua Xiao
Yonghai Liu
Deqin Geng
机构
[1] Affiliated Hospital of Xuzhou Medical College,Department of Neurology
[2] Nanjing Medical University,Department of Emergency Medicine, Huai’an First People’s Hospital
[3] Soochow University,Department of Neurology, The Second Affiliated Hospital of Soochow University
[4] Xuzhou Medical College,Department of Pathogenic Biology and Lab of Infection and Immunology
[5] Affiliated Hospital of Jining Medical University,Department of Neurology
来源
Clinical and Experimental Medicine | 2016年 / 16卷
关键词
MicroRNAs; Myasthenia gravis; MiR-181c; IL-7; IL-17;
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学科分类号
摘要
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.
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页码:413 / 421
页数:8
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