Hepatitis C virus core protein induces hepatic steatosis via Sirt1-dependent pathway

Liver Int. 2018 May;38(5):803-812. doi: 10.1111/liv.13581. Epub 2017 Oct 4.

Abstract

Background & aims: Hepatic steatosis is a common feature of patients with chronic hepatitis C. Previous reports have shown that the overexpression of hepatitis C virus core-encoding sequences (hepatitis C virus genotypes 3a and 1b) significantly induces intracellular triglyceride accumulation. However, the underlying mechanism has not yet been revealed.

Methods: To investigate whether Sirt1 is involved in hepatitis C virus-mediated hepatic steatosis, the overexpression of hepatitis C virus core 1b protein and Sirt1 and the knockdown of Sirt1 in HepG2 cells were performed. To confirm the results of the cellular experiment liver-specific Sirt1 KO mice with lentivirus-mediated hepatitis C virus core 1b overexpression were studied.

Results: Our results show that hepatitis C virus core 1b protein overexpression led to the accumulation of triglycerides in HepG2 cells. Notably the expression of PPARγ2 was dramatically increased at both the mRNA and protein levels by hepatitis C virus core 1b overexpression. The protein expression of Sirt1 is an upstream regulator of PPARγ2 and was also significantly increased after core 1b overexpression. In addition, the overexpression or knockdown of Sirt1 expression alone was sufficient to modulate p300-mediated PPARγ2 deacetylation. In vivo studies showed that hepatitis C virus core protein 1b-induced hepatic steatosis was attenuated in liver-specific Sirt1 KO mice by downregulation of PPARγ2 expression.

Conclusions: Sirt1 mediates hepatitis C virus core protein 1b-induced hepatic steatosis by regulation of PPARγ2 expression.

Keywords: PPARγ2; Sirt1; deacetylation; hepatitis C virus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Fatty Liver / genetics
  • Fatty Liver / metabolism*
  • Fatty Liver / virology
  • Gene Expression
  • Hep G2 Cells
  • Hepacivirus
  • Hepatitis C, Chronic / complications
  • Humans
  • Liver / pathology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • PPAR gamma / metabolism
  • RNA, Messenger / metabolism
  • Sirtuin 1 / genetics*
  • Triglycerides / metabolism
  • Viral Core Proteins / metabolism*

Substances

  • PPAR gamma
  • RNA, Messenger
  • Triglycerides
  • Viral Core Proteins
  • nucleocapsid protein, Hepatitis C virus
  • Sirt1 protein, mouse
  • Sirtuin 1