IL-6, IL-17 and STAT3: a holy trinity in auto-immunity?

被引:138
|
作者
Camporeale, Annalisa [1 ]
Poli, Valeria [1 ]
机构
[1] Univ Turin, Ctr Mol Biotechnol, I-10126 Turin, Italy
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2012年 / 17卷
关键词
IL-6; STAT3; Auto-immunity; sIL-6R; Cytokines; Th17; Review; ACUTE-PHASE RESPONSE; REGULATORY T-CELLS; MESSENGER-RNA EXPRESSION; RHEUMATOID-ARTHRITIS PATIENTS; INFLAMMATORY-BOWEL-DISEASE; MULTIPLE-SCLEROSIS LESIONS; COLLAGEN-INDUCED ARTHRITIS; ANTIGEN-INDUCED ARTHRITIS; ZYMOSAN-INDUCED ARTHRITIS; IFN-GAMMA;
D O I
10.2741/4054
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
Interleukin-6 (IL-6) is a pleiotropic cytokine involved in the regulation of the cross talk between haematopoietic/immune cells and stromal cells, including the onset and resolution of inflammation, responses to infection, tissue remodelling and cancer. It is produced, among others, by fibroblasts, endothelial cells, macrophages and lymphocytes. IL-6 can interact with both membrane-bound and soluble forms of its ligand-binding receptor, the IL-6Ralpha, triggering signalling via dimerization of gp130, the signalling subunit of the IL-6 receptor complex. This leads to the activation of the JAK/STAT pathway and mainly culminates in the activation of the STAT3 transcription factor. Both IL-6 and STAT3 have recently emerged as main regulators of the differentiation and function of Th17 cells, via a positive feedback loop enhancing expression and/or activation of IL-6 itself, IL-17 and STAT3. Dysregulated IL-6 production and signalling are associated with chronic inflammatory diseases, auto-immunity and cancer, and are the object of intense translational research as promising therapeutic targets.
引用
收藏
页码:2306 / 2326
页数:21
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