Bifurcation of Toll-like receptor 9 signaling by adaptor protein 3.

Science

Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA.

Published: September 2010

AI Article Synopsis

  • TLRs 7 and 9 in endosomes detect viral pathogens and trigger signals that activate proinflammatory cytokines and type I interferons.
  • TLR9 specifically requires its movement to a unique lysosome-related organelle for signaling type I interferon, while proinflammatory cytokine signaling does not depend on this trafficking.
  • The study identifies adapter protein-3 as the key player responsible for transporting TLR9 to this specialized compartment, highlighting a complex mechanism for differentiating TLR9's signaling pathways.

Article Abstract

Endosomal Toll-like receptors (TLRs) 7 and 9 recognize viral pathogens and induce signals leading to the activation of nuclear factor κB (NF-κB)-dependent proinflammatory cytokines and interferon regulatory factor 7 (IRF7)-dependent type I interferons (IFNs). Recognition of viral nucleic acids by TLR9 requires its cleavage in the endolysosomal compartment. Here, we show that TLR9 signals leading to the activation of type I IFN, but not proinflammatory cytokine genes, require TLR9 trafficking from endosomes to a specialized lysosome-related organelle. Furthermore, we identify adapter protein-3 as the protein complex responsible for the trafficking of TLR9 to this subcellular compartment. Our results reveal an intracellular mechanism for bifurcation of TLR9 signals by selective receptor trafficking within the endosomal system.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063333PMC
http://dx.doi.org/10.1126/science.1187029DOI Listing

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