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

  1. Zhaohua Zhong1
  1. 1Department of Microbiology, Harbin Medical University, Harbin 150081, China
  2. 2Department of Cell Biology, Harbin Medical University, Harbin 150081, China
  3. 3Department of Cardiology, The First Hospital of Harbin Medical University, Harbin 150001, China
  1. Corresponding authors: zhongzh{at}hrbmu.edu.cn, zhongwr{at}ems.hrbmu.edu.cn

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.

Keywords

  • Received May 20, 2019.
  • Accepted October 28, 2019.

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