Chicken miR-126-5p negatively regulates antiviral innate immunity by targeting TRAF3

被引:0
作者
Jie Wang
Yuqiang Cheng
Longlong Wang
Aixi Sun
Zhenyu Lin
Wenxian Zhu
Zhaofei Wang
Jingjiao Ma
Henan Wang
Yaxian Yan
Jianhe Sun
机构
[1] Shanghai Jiao Tong University,Shanghai Key Laboratory of Veterinary Biotechnology, Key Laboratory of Urban Agriculture (South), Ministry of Agriculture, School of Agriculture and Biology
[2] Shanghai Yuan Song Biotechnology Co.,undefined
[3] LTD.,undefined
来源
Veterinary Research | / 53卷
关键词
Chicken; miR-126-5p; TRAF3; RNA viruses; innate immunity;
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摘要
Innate immunity plays an essential role in preventing the invasion of pathogenic microorganisms. However, innate immunity is a double-edged sword, whose excessive activation is detrimental to immune homeostasis and even leads to a “cytokine storm” of the infected host. The host develops a series of negative regulatory mechanisms to balance the immune response. Here, we report a negative regulatory mechanism of chicken innate immunity mediated by miRNA. In the GEO database, we found that miR-126-5p was markedly up-regulated in chickens infected by RNA viruses. Upregulation of miR-126-5p by RNA virus was then further shown via both a cell model and in vivo tests. Overexpression of miR-126-5p significantly inhibited the expression of interferon and inflammatory cytokine-related genes induced by RNA viruses. The opposite result was achieved after the knockdown of miR-126-5p expression. Bioinformatics analysis identified TRAF3 as candidate target gene of miR-126-5p. Experimentally, miR-126-5p can target TRAF3, as shown by the effects of miR-126-5p on the endogenous expression of TRAF3, and by the TRAF3 3'UTR driven luciferase reporter assay. Furthermore, we demonstrated that miR-126-5p negatively regulated innate immunity by blocking the MAVS-TRAF3-TBK1 axis, with a co-expression assay. Overall, our results suggest that miR-126-5p is involved in the negative regulation of chicken innate immunity, which might contribute to maintaining immune balance.
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