Signalling adaptors used by Toll-like receptors: An update

被引:268
|
作者
Kenny, Elaine F. [1 ]
O'Neill, Luke A. J. [1 ]
机构
[1] Trinity Coll Dublin, Sch Biochem & Immunol, Dublin, Ireland
关键词
Toll-like receptor; Toll/IL1 receptor domain; MyD88; Mal; TRAM;
D O I
10.1016/j.cyto.2008.07.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Research into the five Toll/IL1 receptor (TIR) adaptor proteins involved in innate immunity continues to advance. Here we outline some of the more recent findings. MyD88 has a key role in signalling by the IL1 receptor complex and TLRs. However, a MyD88-independent pathway of IL1 beta signalling in neurons has been described which involves the protein kinase Akt, and which has an anti-apoptotic effect. This pathway may also be important for the mechanism whereby Alum exerts its adjuvant effect since this depends on IL1 beta but is MyD88-independent. MyD88 is also involved in turnourigenesis in models of hepatocarcinoma and familial associated polyposis (FAP); negative regulation of TLR3 signalling and in PKC epsilon activation. The adaptor Mal is regulated by phosphorylation and caspase-1 cleavage. A variant form of Mal in humans termed S180L confers protection in multiple infectious diseases. TRAM is controlled by myristoylation and phosphorylation and the localisation of TRAM with TLR4 to endosomes is required for activation of IRF3 and induction of IFN beta. Finally SARM has been shown to regulate TRIF and also appears to be involved in neuronal injury mediated by oxidative stress in mouse neurons. These advances confirm the importance for the TIR domain-containing adapters in host defence and inflammation. (C) 2008 Published by Elsevier Ltd.
引用
收藏
页码:342 / 349
页数:8
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