The family of Toll-like receptors (TLRs) senses conserved structures found in a broad range of pathogens, causing innate immune responses that include the production of inflammatory cytokines, chemokines and interferons. The signal transduction is initiated from the Toll/interleukin-1 receptor (TIR) domain of TLRs after pathogen recognition. Almost all TLRs use a TIR-containing adapter MyD88 to activate a common signaling pathway that results in the activation of NF-kappaB to express cytokine genes relevant to inflammation. Recently, three further TIR-containing adapters have been identified and shown to selectively interact with several TLRs. In particular, activation of the TRIF-dependent pathway confers antiviral responses by inducing anti-viral genes including that encoding interferon-beta. Taken together, these results indicate that the interaction between individual TLRs and the different combinations of adapters directs appropriate responses against distinct pathogens.
机构:
Univ Paris 07, F-75870 Paris, France
Univ Paris 07, INSERM, U773, Ctr Rech Biomed Bichat Beaujon,CRB3, F-75018 Paris, FranceUniv Paris 07, F-75870 Paris, France
Ogier-Denis, Eric
Ben Mkaddem, Sanae
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机构:
Univ Paris 07, F-75870 Paris, France
Univ Paris 07, INSERM, U773, Ctr Rech Biomed Bichat Beaujon,CRB3, F-75018 Paris, FranceUniv Paris 07, F-75870 Paris, France
Ben Mkaddem, Sanae
Vandewalle, Alain
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Univ Paris 07, F-75870 Paris, France
Univ Paris 07, INSERM, U773, Ctr Rech Biomed Bichat Beaujon,CRB3, F-75018 Paris, FranceUniv Paris 07, F-75870 Paris, France