RAIDD Mediates TLR3 and IRF7 Driven Type I Interferon Production.

  • Experimental and¬†Molecular Immunology
September 08, 2016 By:
  • Maney SK
  • Xu HC
  • Huang J
  • Pandyra AA
  • Ehlting C
  • Aguilar-Valenzuela R
  • Pozdeev VI
  • McIlwain DR
  • Zimmermann A
  • Bode JG
  • Hengel H
  • Kirschning CJ
  • Kim IR
  • Hiscott J
  • Brenner D
  • Haussinger D
  • Ohashi PS
  • Mak TW
  • Lang KS
  • Lang PA.

BACKGROUND/AIMS: Viral infections represent a global health problem with the need for new viral therapies and better understanding of the immune response during infection. The most immediate and potent anti-viral defense mechanism is the production of type I interferon (IFN-I) which are activated rapidly following recognition of viral infection by host pathogen recognition receptors (PRR). The mechanisms of innate cellular signaling downstream of PRR activation remain to be fully understood. In the present study, we demonstrate that CASP2 and RIPK1 domain-containing adaptor with death domain (CRADD/RAIDD) is a critical component in type I IFN production. METHODS: The role of RAIDD during IFN-I production was investigated using western blot, shRNA mediated lentiviral knockdown, immunoprecipitation and IFN-I driven dual luciferase assay. RESULTS: Immunoprecipitation analysis revealed the molecular interaction of RAIDD with interferon regulatory factor 7 (IRF7) and its phosphorylating kinase IKKepsilon. Using an IFN-4alpha driven dual luciferase analysis in RAIDD deficient cells, type I IFN activation by IKKepsilon and IRF7 was dramatically reduced. Furthermore, deletion of either the caspase recruitment domain (CARD) or death domain (DD) of RAIDD inhibited IKKepsilon and IRF7 mediated interferon-4alpha activation. CONCLUSION: We have identified that the adaptor molecule RAIDD coordinates IKKepsilon and IRF7 interaction to ensure efficient expression of type I interferon.

2016 Sep. Cell Physiol Biochem.39(4):1271-80. Epub 2016 Sep 8.
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