4.7 Article

TIRAP: an adapter molecule in the Toll signaling pathway

Journal

NATURE IMMUNOLOGY
Volume 2, Issue 9, Pages 835-841

Publisher

NATURE AMERICA INC
DOI: 10.1038/ni0901-835

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Funding

  1. NIAID NIH HHS [AI44220-01] Funding Source: Medline

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Mammalian Toll-like receptors (TLRs) recognize conserved products of microbial metabolism and activate NF-kappaB and other signaling pathways through the adapter protein MyD88. Although some cellular responses are completely abolished in MyD88-deficient mice, TLR4, but not TLR9, can activate NF-KB and mitogen-activated protein kinases and induce dendritic cell maturation in the absence of MyD88. These differences suggest that another adapter must exist that can mediate MyD88-independent signaling in response to TLR4 ligation. We have identified and characterized a Toll-interleukin I receptor (TIR) domain-containing adapter protein (TIRAP) and have shown that it controls activation of MyD88-independent signaling pathways downstream of TLR4. We have also shown that the double-stranded RNA-binding protein kinase PKR is a component of both the TIRAP- and MyD88-dependent signaling pathways.

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