4.7 Article

TRAM couples endocytosis of Toll-like receptor 4 to the induction of interferon-beta

Journal

NATURE IMMUNOLOGY
Volume 9, Issue 4, Pages 361-368

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ni1569

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Funding

  1. Howard Hughes Medical Institute Funding Source: Medline
  2. NIAID NIH HHS [AI 061360, U01 AI061360, P01 AI044220, R00 AI072955-02, P01 AI44220, R01 AI046688, R00 AI072955, K99 AI072955, K99 AI072955-01, 1K99AI072955-01, R37 AI046688] Funding Source: Medline
  3. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R37AI046688, P01AI044220, K99AI072955, U01AI061360, R00AI072955, R01AI046688] Funding Source: NIH RePORTER

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Toll-like receptor 4 (TLR4) induces two distinct signaling pathways controlled by the TIRAP-MyD88 and TRAM-TRIF pairs of adaptor proteins, which elicit the production of proinflammatory cytokines and type I interferons, respectively. How TLR4 coordinates the activation of these two pathways is unknown. Here we show that TLR4 activated these two signaling pathways sequentially in a process organized around endocytosis of the TLR4 complex. We propose that TLR4 first induces TIRAP-MyD88 signaling at the plasma membrane and is then endocytosed and activates TRAM-TRIF signaling from early endosomes. Our data emphasize a unifying theme in innate immune recognition whereby all type I interferon-inducing receptors signal from an intracellular location.

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