MiR-146a down-regulates inflammatory response by targeting TLR3 and TRAF6 in Coxsackievirus B infection

Author:

Fei Yanru,Chaulagain Anita,Wang Tianying,Chen Yang,Liu Jinchang,Yi Ming,Wang Ying,Huang Yike,Lin Lexun,Chen Sijia,Xu Weizhen,Tong Lei,Wu Xiaoyu,Zhao Dechao,Zhang Fengmin,Zhao Wenran,Zhong Zhaohua

Abstract

Coxsackievirus B (CVB) is the major cause of human myocarditis and dilated cardiomyopathy. Toll-like receptor 3 (TLR3) is an intracellular sensor to detect pathogen's dsRNA. TLR3, along with TRAF6, triggers an inflammatory response through NF-κB signaling pathway. In the cells infected with CVB type 3 (CVB3), the abundance of miR-146a was significantly increased. The role of miR-146a in CVB infection is unclear. In this study, TLR3 and TRAF6 were identified as the targets of miR-146a. The elevated miR-146a inhibited NF-κB translocation and subsequently down-regulated proinflammatory cytokine expression in the CVB3-infected cells. Therefore, the NF-κB pathway can be doubly blocked by miR-146a through targeting of TLR3 and TRAF6. MiR-146a may be a negative regulator on inflammatory response and an intrinsic protective factor in CVB infection.

Funder

National Natural Science Foundation of China

China Scholarship Council

Government of Nepal, Ministry of Education

Heilongjiang Province Graduate Innovation Research

University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province

Health Commission of Heilongjiang Province

Publisher

Cold Spring Harbor Laboratory

Subject

Molecular Biology

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