FEBS Letters · 2011 · 14 citations · 43 references
Life SciencesImmunologyMolecular BiologyGene ExpressionInflammationInnate ImmunityCytokine BiologyInflammatory Cell ResponsesInflammatory SignalingInnate Immune ResponseInnate Immune Signaling PathwaysInterferon ResponsesInterferon Response To Viral InfectionInterferon Signaling ResponsesInterferon-induced GenesS100 Protein ExpressionS100 ProteinsType I Interferon Pathways
Viral double-stranded RNA (dsRNA) and its synthetic analog polyI:C are recognized via multiple pathways and induce the expression of genes related to inflammation. In the present study, we demonstrated the polyI:C-induced gene expression of the damage associated molecular pattern (DAMP) molecules S100A8 and S100A9, while other S100 genes were not affected. Cycloheximide and Brefeldin A treatment revealed both the expression of S100A8 and S100A9 as secondary response genes and the involvement of polyI:C-induced cytokines herein. Several type I and type III interferons such as IFNβ, IL-20, IL-24, and IFNλ/IL-29 were expressed in response to polyI:C, however, they failed to induce S100A8 and S100A9 gene expression. These data indicate the involvement of the danger molecule S100A8/A9 in the resistance against viruses.
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IRF3 Mediates a TLR3/TLR4-Specific Antiviral Gene Program
Sean E. Doyle, Sagar A. Vaidya, Ryan M. O’Connell et al. · Immunity · 2002 · 837 citations · Full text