DUSP4 modulates RIG-I- and STING-mediated IRF3-type I IFN response

Cell Death Differ. 2024 Mar;31(3):280-291. doi: 10.1038/s41418-024-01269-7. Epub 2024 Feb 21.

Abstract

Detection of cytosolic nucleic acids by pattern recognition receptors, including STING and RIG-I, leads to the activation of multiple signalling pathways that culminate in the production of type I interferons (IFNs) which are vital for host survival during virus infection. In addition to protective immune modulatory functions, type I IFNs are also associated with autoimmune diseases. Hence, it is important to elucidate the mechanisms that govern their expression. In this study, we identified a critical regulatory function of the DUSP4 phosphatase in innate immune signalling. We found that DUSP4 regulates the activation of TBK1 and ERK1/2 in a signalling complex containing DUSP4, TBK1, ERK1/2 and IRF3 to regulate the production of type I IFNs. Mice deficient in DUSP4 were more resistant to infections by both RNA and DNA viruses but more susceptible to malaria parasites. Therefore, our study establishes DUSP4 as a regulator of nucleic acid sensor signalling and sheds light on an important facet of the type I IFN regulatory system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Immunity, Innate
  • Interferon Type I* / metabolism
  • Membrane Proteins* / metabolism
  • Mice
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Tyrosine Phosphatases* / metabolism
  • Receptors, Cell Surface* / metabolism
  • Roundabout Proteins* / metabolism
  • Signal Transduction
  • Virus Diseases* / immunology
  • Virus Diseases* / metabolism

Substances

  • Interferon Type I
  • Protein Serine-Threonine Kinases
  • MKP2 protein, mouse
  • Robo3 protein, mouse
  • Sting1 protein, mouse
  • Membrane Proteins
  • Roundabout Proteins
  • Protein Tyrosine Phosphatases
  • Receptors, Cell Surface