A type I interferon-mitochondrial axis regulates efferocytosis and interferon-stimulated gene induction in macrophages

Immunity. 2026 Feb 10;59(2):306-321.e7. doi: 10.1016/j.immuni.2025.12.010. Epub 2026 Jan 28.

Abstract

Macrophage metabolism is intricately linked to cellular function. Contrasting with Toll-like receptor (TLR) stimulation, cytosolic nucleic acid sensing induced a decrease in mitochondrial membrane potential (MMP) while maintaining mitochondrial respiration. Interferon α/β (IFN-I) receptor (IFNAR) signaling was necessary and sufficient for this metabolic response. IFNAR signaling induced interferon-stimulated gene 15 (ISG15) expression and ISGylation of mitochondrial proteins, including subunits of mitochondrial complex V, increasing ATP production and decreasing MMP, thus enhancing macrophage efferocytic capacity. Moreover, the IFNAR-ISG15-mediated drop in MMP activated the mitochondrial protease OMA1, inducing mitochondrial fission and decreasing endoplasmic reticulum-mitochondria communication, thus dampening IFN-stimulated gene (ISG) induction. Loss of ISG15 or OMA1 enhanced histone acetylation and ISG induction upon IFN-I stimulation, in a manner dependent on mitochondrial calcium uptake. This increase in ISG induction provided protection against acute viral infections. These data indicate that IFNAR-ISG15 signaling boosts efferocytosis while limiting ISG induction, thereby promoting the resolution of inflammation.

Keywords: efferocytosis; interferon-stimulated genes; macrophage; metabolism; mitochondrial endoplasmic reticulum contacts; mitochondrial fission; mitochondrial membrane potential; oxidative phosphorylation; type I interferon; viral infection.

MeSH terms

  • Animals
  • Cytokines / genetics
  • Cytokines / metabolism
  • Efferocytosis
  • Humans
  • Interferon Type I* / immunology
  • Interferon Type I* / metabolism
  • Macrophages* / immunology
  • Macrophages* / metabolism
  • Membrane Potential, Mitochondrial
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mitochondria* / immunology
  • Mitochondria* / metabolism
  • Phagocytosis* / immunology
  • Receptor, Interferon alpha-beta / genetics
  • Receptor, Interferon alpha-beta / metabolism
  • Signal Transduction

Substances

  • Interferon Type I
  • Receptor, Interferon alpha-beta
  • Cytokines