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技術(shù)文章

士鋒生物:白介素17誘導的信號通路圖

點擊次數(shù):2724 發(fā)布時間:2013-7-22

Structure and signalling in the IL-17 receptor family

Schematic depicting interleukin-17 receptor (IL-17R) signalling. The IL-17R complex is composed of IL-17RA and IL-17RC. Both subunits encode SEF/IL-17R (SEFIR) domains, but a sequence similar to the Toll/IL-1R (TIR) BB-loop is found only in IL-17RA, termed a TIR-like loop (TILL). IL-17RA engages the SEFIR domain-containing adaptor ACT1 to mediate various downstream events. Specifically, ACT1 is required for recruitment of TNFR-associated factor 6 (TRAF6) and possibly TRAF3, which are essential upstream activators of the canonical nuclear factor-κB (NF-κB) pathway. It is not clear whether TRAF6 is also required for the activation of the mitogen-activated protein kinase (MAPK) p38. Act1-/- cells fail to upregulate the expression of the liver-enriched activator protein (LAP) and LAP* splice variants of CCAAT/enhancer-binding protein-β(C/EBPβ) or the expression of C/EBPδ, another event that might be downstream of NF-κB. ACT1, but not TRAF6, is required for IL-17A-induced stabilization of several target mRNAs, particularly those encoding chemokines and cytokines. Interestingly, extracellular signal-regulated kinase (ERK) might also be controlled, at least indirectly, by ACT1-independent pathways, as Act1-/- cells show strong upregulation of ERK phosphorylation 24 hours after IL-17A stimulation. ERK mediates rapid phosphorylation of C/EBPβon threonine 188 . A second functional domain on IL-17RA is located in the carboxy-terminal region and is not required for efficient activation of NF-κB and MAPK pathways. However, deletion of this domain results in impaired alternative translation of C/EBPβfrom the LAP isoform to the LAP* isoform, and hence was termed the C/EBPβ-activation domain (CBAD). The CBAD is also required for IL-17A-mediated inducible phosphorylation of C/EBPβon threonine 179, which is mediated by glycogen synthase kinase 3β(GSK3β). b | Comparison of IL-17R and Toll-like receptor (TLR) signalling. IL-17R and TLR (or IL-1R, not shown) signalling pathways use different functional receptor motifs (SEFIR and TILL versus Toll/IL-1R (TIR) domains) and proximal adaptors (ACT1 versus MYD88 (myeloid differentiation primary-response protein 88) and TRIF (TIR-domain-containing adaptor protein inducing IFNβ)), but converge on common pathways (NF-κB, C/EBP and MAPKs). Therefore, these receptors activate similar, although not identical, panels of downstream genes. IκBξ, inhibitor of NF-κB-ξ; IRF3, interferon regulatory factor 3; P13K, phosphoinositide 3-kinase.

IL 17 Signaling Pathway

IL-17R家族的配體 - 受體關(guān)系和主要結(jié)構(gòu)特點IL-17R family ligand–receptor relationships and main structural features

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