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Tuesday 8 January 2008

Toll-like receptor-4 (TLR4) is the endotoxin receptor.

The sepsis syndrome is thought to occur when microbial products activate Toll-like receptors stimulating widespread inflammation, in turn causing organ failure, shock and death. Not only microbial substances but also endogenous molecules can trigger Toll-like receptors.

Toll-like receptor-4 (TLR4), the endotoxin receptor, is constitutively suppressed. The first step in sepsis could be the release of Toll-like receptor-4 from suppression.

TLR4 signaling pathway

TLR4 activates both the MyD88- and the TRIF-dependent pathways. TIRAP and TRAM are required for the activation of the MyD88- and the TRIF-dependent pathways, respectively. MyD88 recruits TRAF6 and members of the IRAK family. TRAF6, together with Ubc13 and Uev1A, activates the TAK1 complex via K63-linked ubiquitination (Ub).

The activated TAK1 complex then activates the IKK complex consisting of IKKα, IKKβ and NEMO, which catalyzes the phosphorylation of IκB proteins (P). IκBs are destroyed by the proteasome-dependent pathway, allowing NF-κB (RelA–p50 heterodimer) to translocate into the nucleus (canonical pathway).

Simultaneously, the TAK1 complex activates the MAPK pathway, which results in the phosphorylation (P) and activation of AP-1. NF-κB and AP-1 control inflammatory responses through the induction of inflammatory cytokines. TRIF recruits TRAF3, which then interacts with TBK1 and IKKi. These kinases mediate phosphorylation of IRF3 (P).

Phosphorylated IRF3 dimerizes and translocates into the nucleus to regulate transcription. TRIF also interacts with TRAF6 and RIP1, which mediate NF-κB activation.

Activation of the IRF3, NF-κB and MAPK pathways is required for induction of type I IFN, particularly IFN-β. There are two types of NF-κB activation in TLR4 signaling: the MyD88-dependent pathway, which mediates early phase activation of NF-κB and the TRIF-dependent pathway, which mediates the late phase activation of NF-κB.


- variants in

See also

- TLRs


- Brunn GJ, Platt JL. The etiology of sepsis: turned inside out. Trends Mol Med. 2005 Nov 17; PMID: 16298551


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