MicroRNA-146a Contributes to SCI Recovery via Regulating TRAF6 and IRAK1 Expression

Biomed Res Int. 2016:2016:4013487. doi: 10.1155/2016/4013487. Epub 2016 Oct 17.

Abstract

MicroRNA-146a participates in spinal cord injury (SCI) recovery. Until recently, how miRNA-146a participates in SCI remained unclear. In this study, we tried to explore the roles of miRNA-146a in the recovery of SCI using a rat model. The expression of the probable target genes of miRNA-146a (including IRAK1 and TARF6) as well as proinflammation cytokines were measured until 7 days after surgery in the three groups (sham group, SCI group, and miRNA-146a antagomir injection group). Also, the animals' motivations were estimated using Basso Beattie Bresnahan (BBB) during the whole experiment. A luciferase assay was performed to demonstrate that miRNA-146a could directly target the mRNAs of IRAK1 and TRAF6. Our experiments indicate that miRNA-146a inhibits proinflammatory cytokine secretion by suppressing IRAK1 and TRAF6 expression in the SCI model. In contrast, miRNA-146a may be upregulated by inflammatory mediators via the IRAK1/TRAF6 pathway in the spinal cord. As a negative feedback element, miRNA-146a could make sure that the expression of IRAK1- and TRAF6-mediated genes was under tight control. Thus, miRNA-146a may serve as a novel therapeutic target for SCI interventions.

MeSH terms

  • Animals
  • Female
  • Gene Expression Regulation*
  • Interleukin-1 Receptor-Associated Kinases / metabolism*
  • MicroRNAs / metabolism*
  • Rats
  • Rats, Wistar
  • Recovery of Function*
  • Spinal Cord Injuries / physiopathology*
  • TNF Receptor-Associated Factor 6 / metabolism*
  • Thoracic Vertebrae / injuries

Substances

  • MIRN146 microRNA, rat
  • MicroRNAs
  • TNF Receptor-Associated Factor 6
  • IRAK1 protein, rat
  • Interleukin-1 Receptor-Associated Kinases