The potential of adiponectin in driving arthritis

被引:228
作者
Ehling, Angela
Schaeffler, Andreas
Herfarth, Hans
Tarner, Ingo H.
Anders, Sven
Distler, Oliver
Paul, Gisela
Distler, Joerg
Gay, Steffen
Schoelmerich, Jurgen
Neumann, Elena
Mueller-Ladner, Ulf
机构
[1] Univ Hosp Giessen, Dept Rheumatol & Clin Immunol, Kerckhoff Klin, Bad Nauheim, Germany
[2] Univ Hosp Regensburg, Dept Internal Med 1, Regensburg, Germany
[3] Univ Hosp Regensburg, Dept Orthoped, Regensburg, Germany
[4] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[5] Univ Zurich Hosp, Ctr Expt Rheumatol, CH-8091 Zurich, Switzerland
关键词
D O I
10.4049/jimmunol.176.7.4468
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Articular adipose tissue is a ubiquitous component of human joints, but its local functions are largely unknown. Because recent studies revealed several links between adipose tissue, adipocytokines, and arthritis, we investigated the expression of the adipocytokine adiponectin and its functional role in articular adipose tissue and synovium of patients with different arthritides. In contrast to its protective role in endocrinological and vascular diseases, adiponectin was found to be involved in key pathways of inflammation and matrix degradation in the human joint. The effects of adiponectin in human synovial fibroblasts appear to be highly selective by inducing only two of the main mediators of rheumatoid arthritis pathophysiology, IL-6 and matrix metalloproteinase-1, via the p38 MAPK pathway. Owing to the observation that these effects could be inhibited by different TNF-alpha inhibitors, adipocytokines such as adiponectin may also be key targets for therapeutic strategies in inflammatory joint diseases. In summary, articular adipose tissue and adipocytokines cannot be regarded as innocent bystanders any more in chronic inflammatory diseases such as arthritis.
引用
收藏
页码:4468 / 4478
页数:11
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