Activation of the cGAS-STING-IRF3 Axis by Type I and II Interferons Contributes to Host Defense

Adv Sci (Weinh). 2024 Sep;11(35):e2308890. doi: 10.1002/advs.202308890. Epub 2024 Jul 14.

Abstract

Interferons (IFNs) activate JAK-STAT pathways to induce downstream effector genes for host defense against invaded pathogens and tumors. Here both type I (β) and II (γ) IFNs are shown that can activate the transcription factor IRF3 in parallel with STAT1. IRF3-deficiency impairs transcription of a subset of downstream effector genes induced by IFN-β and IFN-γ. Mechanistically, IFN-induced activation of IRF3 is dependent on the cGAS-STING-TBK1 axis. Both IFN-β and IFN-γ cause mitochondrial DNA release into the cytosol. In addition, IFNs induce JAK1-mediated tyrosine phosphorylation of cGAS at Y214/Y215, which is essential for its DNA binding activity and signaling. Furthermore, deficiency of cGAS, STING, or IRF3 impairs IFN-β- or IFN-γ-mediated antiviral and antitumor activities. The findings reveal a novel IRF3 activation pathway parallel with the canonical STAT1/2 activation pathways triggered by IFNs and provide an explanation for the pleiotropic roles of the cGAS-STING-IRF3 axis in host defense.

Keywords: JAK‐STATs; antitumor; antiviral responses; cGAS‐STING‐IRF3; interferon; phosphorylation.

MeSH terms

  • Animals
  • Humans
  • Interferon Regulatory Factor-3* / genetics
  • Interferon Regulatory Factor-3* / metabolism
  • Interferon Type I / genetics
  • Interferon Type I / metabolism
  • Interferon-beta / genetics
  • Interferon-beta / metabolism
  • Interferon-gamma / genetics
  • Interferon-gamma / immunology
  • Interferon-gamma / metabolism
  • Membrane Proteins* / genetics
  • Membrane Proteins* / metabolism
  • Mice
  • Nucleotidyltransferases* / genetics
  • Nucleotidyltransferases* / metabolism
  • STAT1 Transcription Factor / genetics
  • STAT1 Transcription Factor / metabolism
  • Signal Transduction*

Substances

  • Nucleotidyltransferases
  • Interferon Regulatory Factor-3
  • Membrane Proteins
  • cGAS protein, mouse
  • Interferon-gamma
  • Irf3 protein, mouse
  • Sting1 protein, mouse
  • Interferon Type I
  • cGAS protein, human
  • STAT1 Transcription Factor
  • Interferon-beta
  • STING1 protein, human
  • IRF3 protein, human