MicroRNA-302 Cluster Downregulates Enterovirus 71-Induced Innate Immune Response by Targeting KPNA2

J Immunol. 2018 Jul 1;201(1):145-156. doi: 10.4049/jimmunol.1701692. Epub 2018 May 18.

Abstract

Enterovirus 71 (EV71) induces significantly elevated levels of cytokines and chemokines, leading to local or systemic inflammation and severe complications. As shown in our previous study, microRNA (miR) 302c regulates influenza A virus-induced IFN expression by targeting NF-κB-inducing kinase. However, little is known about the role of the miR-302 cluster in EV71-mediated proinflammatory responses. In this study, we found that the miR-302 cluster controls EV71-induced cytokine expression. Further studies demonstrated that karyopherin α2 (KPNA2) is a direct target of the miR-302 cluster. Interestingly, we also found that EV71 infection upregulates KPNA2 expression by downregulating miR-302 cluster expression. Upon investigating the mechanisms behind this event, we found that KPNA2 intracellularly associates with JNK1/JNK2 and p38, leading to translocation of those transcription factors from the cytosol into the nucleus. In EV71-infected patients, miR-302 cluster expression was downregulated and KPNA2 expression was upregulated compared with controls, and their expression levels were closely correlated. Taken together, our work establishes a link between the miR-302/ KPNA2 axis and EV71-induced cytokine expression and represents a promising target for future antiviral therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus / physiology
  • Cell Line, Tumor
  • Cytokines / metabolism*
  • Enterovirus A, Human / immunology*
  • HEK293 Cells
  • Humans
  • Immunity, Innate / immunology*
  • MicroRNAs / biosynthesis
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Mitogen-Activated Protein Kinase 8 / metabolism
  • Mitogen-Activated Protein Kinase 9 / metabolism
  • THP-1 Cells
  • Transcription Factor RelA / metabolism
  • alpha Karyopherins / biosynthesis
  • alpha Karyopherins / metabolism*
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Cytokines
  • KPNA2 protein, human
  • MIRN302A microRNA, human
  • MicroRNAs
  • RELA protein, human
  • Transcription Factor RelA
  • alpha Karyopherins
  • Mitogen-Activated Protein Kinase 9
  • Mitogen-Activated Protein Kinase 8
  • p38 Mitogen-Activated Protein Kinases