Macrophages activated by hepatitis B virus have distinct metabolic profiles and suppress the virus via IL-1β to downregulate PPARα and FOXO3

Cell Rep. 2022 Jan 25;38(4):110284. doi: 10.1016/j.celrep.2021.110284.

Abstract

Macrophages display phenotypic plasticity and can be induced by hepatitis B virus (HBV) to undergo either M1-like pro-inflammatory or M2-like anti-inflammatory polarization. Here, we report that M1-like macrophages stimulated by HBV exhibit a strong HBV-suppressive effect, which is diminished in M2-like macrophages. Transcriptomic analysis reveals that HBV induces the expression of interleukin-1β (IL-1β) in M1-like macrophages, which display a high oxidative phosphorylation (OXPHOS) activity distinct from that of conventional M1-like macrophages. Further analysis indicates that OXPHOS attenuates the expression of IL-1β, which suppresses the expression of peroxisome proliferator-activated receptor α (PPARα) and forkhead box O3 (FOXO3) in hepatocytes to suppress HBV gene expression and replication. Moreover, multiple HBV proteins can induce the expression of IL-1β in macrophages. Our results thus indicate that macrophages can respond to HBV by producing IL-1β to suppress HBV replication. However, HBV can also metabolically reprogram macrophages to enhance OXPHOS to minimize this host antiviral response.

Keywords: IL-1β signaling; M1-like and M2-like macrophages; hepatitis B virus; metabolic reprogramming; oxidative phosphorylation; transcriptional regulation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Down-Regulation
  • Forkhead Box Protein O3 / immunology*
  • Forkhead Box Protein O3 / metabolism
  • Hepatitis B / immunology*
  • Hepatitis B virus
  • Host-Pathogen Interactions / immunology
  • Humans
  • Interleukin-1beta / immunology*
  • Interleukin-1beta / metabolism
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Macrophages / virology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • PPAR gamma / immunology*
  • PPAR gamma / metabolism
  • Virus Replication / immunology

Substances

  • Forkhead Box Protein O3
  • Interleukin-1beta
  • PPAR gamma