Regulation of TLR3 activation by S100A9

Su Yu Tsai, Jesus A. Segovia, Te Hung Chang, Niraj K. Shil, Swechha M. Pokharel, T. R. Kannan, Joel B. Baseman, Joan Defrêne, Nathalie Pagé, Annabelle Cesaro, Philippe A. Tessier, Santanu Bose

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Recognition of viral dsRNA by endosomal TLR3 activates innate immune response during virus infection. Trafficking of TLR3 to the endolysosomal compartment arising from fusion of late endosome (LE) with lysosome is required for recognition and detection of pathogen associated molecular patterns, which results in activation of the TLR3-dependent signaling cascade. Existing knowledge about the mechanism(s) and cellular factor(s) governing TLR3 trafficking is limited. In the current study, we identified intracellular S100A9 protein as a critical regulator of TLR3 trafficking. S100A9 was required for maturation of TLR3 containing early endosome (EE) into LE, the compartment that fuses with lysosome to form the endolysosomal compartment. A drastic reduction in cytokine production was observed in S100A9-knockout (KO) primary macrophages following RNA virus infection and treatment of cells with polyinosinic-polycytidylic acid (polyIC; a dsRNA mimetic that acts as a TLR3 agonist). Mechanistic studies revealed colocalization and interaction of S100A9 with TLR3 following polyIC treatment. S100A9-TLR3 interaction was critical for maturation of TLR3 containing EE into LE because TLR3 could not be detected in the LE of polyIC-treated S100A9-KO macrophages. Subsequently, TLR3 failed to colocalize with its agonist (i.e., biotin-labeled polyIC) in S100A9-deficient macrophages. The in vivo physiological role of S100A9 was evident from loss of cytokine production in polyIC-treated S100A9-KO mice. Thus, we identified intracellular S100A9 as a regulator of TLR3 signaling and demonstrated that S100A9 functions during pre-TLR3 activation stages by facilitating maturation of TLR3 containing EE into LE.

Original languageEnglish (US)
Pages (from-to)4426-4437
Number of pages12
JournalJournal of Immunology
Volume195
Issue number9
DOIs
StatePublished - Nov 2015

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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