Human activated CD4+ T lymphocytes increase IL-2 expression by downregulating microRNA-181c

被引:68
|
作者
Xue, Qian [1 ]
Guo, Zhang-Yan [1 ]
Li, Wei [1 ]
Wen, Wei-Hong [1 ]
Meng, Yan-Ling [1 ]
Jia, Lin-Tao [2 ]
Wang, Jian [3 ]
Yao, Li-Bo [2 ]
Jin, Bo-Quan [1 ]
Wang, Tao [1 ]
Yang, An-Gang [1 ]
机构
[1] Fourth Mil Med Univ, Dept Immunol, State Key Lab Canc Biol, Xian 710032, Shaanxi, Peoples R China
[2] Fourth Mil Med Univ, Dept Biochem & Mol Biol, Xian 710032, Peoples R China
[3] Fourth Mil Med Univ, Inst Neurosci, Xian 710032, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
miRNA; miR-181c; CD4(+) T cell; Activation; IL-2; NORMAL IMMUNE FUNCTION; DIFFERENTIATION; CELLS; CD28; INFLAMMATION; PROMOTER; SIGNALS; CANCER;
D O I
10.1016/j.molimm.2010.10.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs, a large family of small regulatory RNAs, are posttranscriptional gene regulators that bind mRNA in a sequence-specific manner, thereby controlling diverse aspects of cell function, including immune reaction. In this study, we screened and identified a group of differentially expressed miRNAs in naive and activated CD4(+) T cells. Among the miRNAs studied, miR-181c was proven to have the potential to regulate CD4(+) T cell activation. miR-181c was downregulated in the process of CD4(+) T cell activation, and transfection of miR-181c mimics partially repressed the activation of both Jurkat cells and human peripheral blood mononuclear cells (PBMC) CD4(+) T cells. We further showed that miR-181c can bind to the IL-2 3' UTR and repress its expression by inhibiting translation. Moreover, miR-181c mimics reduced activated CD4(+) T cell proliferation. Taken together, our results show that miR-181c serves as a negative regulator that modulates the activation of CD4(+) T cells. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:592 / 599
页数:8
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