VANGL2 inhibits antiviral IFN-I signaling by targeting TBK1 for autophagic degradation.
Stringent control of type I interferon (IFN-I) signaling is critical to potent innate immune responses against viral infection, yet the underlying molecular mechanisms are still elusive. Here, we found that Van Gogh-like 2 (VANGL2) acts as an IFN-inducible negative feedback regulator to suppress IFN-I signaling during vesicular stomatitis virus (VSV) ... infection. Mechanistically, VANGL2 interacted with TBK1 and promoted the selective autophagic degradation of TBK1 via K48-linked polyubiquitination at Lys372 by the E3 ligase TRIP, which serves as a recognition signal for the cargo receptor OPTN. Furthermore, myeloid-specific deletion of VANGL2 in mice showed enhanced IFN-I production against VSV infection and improved survival. In general, these findings revealed a negative feedback loop of IFN-I signaling through the VANGL2-TRIP-TBK1-OPTN axis and highlighted the cross-talk between IFN-I and autophagy in preventing viral infection. VANGL2 could be a potential clinical therapeutic target for viral infectious diseases, including COVID-19.
Mesh Terms:
Animals, Autophagy, Cell Polarity, Interferon Type I, Mice, Protein Serine-Threonine Kinases, Transcription Factors, Virus Diseases
Animals, Autophagy, Cell Polarity, Interferon Type I, Mice, Protein Serine-Threonine Kinases, Transcription Factors, Virus Diseases
Sci Adv
Date: Jun. 23, 2023
PubMed ID: 37352355
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