Literature DB >> 14751757

TLR signaling pathways.

Kiyoshi Takeda1, Shizuo Akira.   

Abstract

Toll-like receptors (TLRs) have been established to play an essential role in the activation of innate immunity by recognizing specific patterns of microbial components. TLR signaling pathways arise from intracytoplasmic TIR domains, which are conserved among all TLRs. Recent accumulating evidence has demonstrated that TIR domain-containing adaptors, such as MyD88, TIRAP, and TRIF, modulate TLR signaling pathways. MyD88 is essential for the induction of inflammatory cytokines triggered by all TLRs. TIRAP is specifically involved in the MyD88-dependent pathway via TLR2 and TLR4, whereas TRIF is implicated in the TLR3- and TLR4-mediated MyD88-independent pathway. Thus, TIR domain-containing adaptors provide specificity of TLR signaling.

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Year:  2004        PMID: 14751757     DOI: 10.1016/j.smim.2003.10.003

Source DB:  PubMed          Journal:  Semin Immunol        ISSN: 1044-5323            Impact factor:   11.130


  752 in total

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3.  Glaucomatous tissue stress and the regulation of immune response through glial Toll-like receptor signaling.

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Journal:  Invest Ophthalmol Vis Sci       Date:  2010-06-10       Impact factor: 4.799

4.  Altered expression of middle and inner ear cytokines in mouse otitis media.

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5.  Pyroglutamylated RF-amide peptide (QRFP) gene is regulated by metabolic endotoxemia.

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Journal:  J Biol Chem       Date:  2013-02-05       Impact factor: 5.157

8.  Blimp-1/PRDM1 mediates transcriptional suppression of the NLR gene NLRP12/Monarch-1.

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10.  Transcriptional regulation of the rat sperm-associated antigen 11e (Spag 11e) gene during endotoxin challenge.

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Journal:  Mol Genet Genomics       Date:  2014-04-29       Impact factor: 3.291

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