Activation of the oncogenic miR-21-5p promotes HCV replication and steatosis induced by the viral core 3a protein

Liver Int. 2019 Jul;39(7):1226-1236. doi: 10.1111/liv.14112. Epub 2019 Apr 16.

Abstract

Background & aims: miR-21-5p is a potent oncogenic microRNA targeting many key tumour suppressors including phosphatase and tensin homolog (PTEN). We recently identified PTEN as a key factor modulated by hepatitis C virus (HCV) to promote virion egress. In hepatocytes, expression of HCV-3a core protein was sufficient to downregulate PTEN and to trigger lipid droplet accumulation. Here, we investigated whether HCV controls PTEN expression through miR-21-5p-dependent mechanisms to trigger steatosis in hepatocytes and to promote HCV life cycle.

Methods: MiR-21-5p expression in HCV-infected patients was evaluated by transcriptome meta-analysis. HCV replication and viral particle production were investigated in Jc1-infected Huh-7 cells after miR-21-5p inhibition. PTEN expression and steatosis were assessed in HCV-3a core protein-expressing Huh-7 cells and in mouse primary hepatocytes having miR-21-5p inhibited or genetically deleted respectively. HCV-3a core-induced steatosis was assessed in vivo in Mir21a knockout mice.

Results: MiR-21-5p expression was significantly increased in hepatic tissues from HCV-infected patients. Infection by HCV-Jc1, or transduction with HCV-3a core, upregulated miR-21-5p expression and/or activity in Huh-7 cells. miR-21-5p inhibition decreased HCV replication and release of infectious virions by Huh-7 cells. HCV-3a core-induced PTEN downregulation and steatosis were further prevented in Huh-7 cells following miR-21-5p inhibition or in Mir21a knockout mouse primary hepatocytes. Finally, steatosis induction by AAV8-mediated HCV-3a core expression was reduced in vivo in Mir21a knockout mice.

Conclusion: MiR-21-5p activation by HCV is a key molecular step, promoting both HCV life cycle and HCV-3a core-induced steatosis and may be among the molecular changes induced by HCV-3a to promote carcinogenesis.

Keywords: hepatitis C; lipid metabolism; microRNA; phosphatase and tensin homolog.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carcinogenesis
  • Cell Line, Tumor
  • Down-Regulation
  • Fatty Liver / metabolism
  • Fatty Liver / pathology
  • Hepacivirus / genetics
  • Hepacivirus / physiology*
  • Hepatocytes / metabolism*
  • Hepatocytes / pathology
  • Hepatocytes / virology*
  • Humans
  • Lipid Metabolism
  • Liver / metabolism
  • Liver / pathology
  • Mice
  • Mice, Knockout
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • PTEN Phosphohydrolase / metabolism*
  • Up-Regulation
  • Viral Core Proteins / physiology*
  • Virus Replication

Substances

  • MIRN-21 microRNA, mouse
  • MIRN21 microRNA, human
  • MicroRNAs
  • Viral Core Proteins
  • nucleocapsid protein, Hepatitis C virus
  • PTEN Phosphohydrolase
  • PTEN protein, human