Osteoarthritis-associated basic calcium phosphate crystals induce pro-inflammatory cytokines and damage-associated molecules via activation of Syk and PI3 kinase

被引:42
作者
Cunningham, Clare C. [1 ]
Mills, Evanna [1 ]
Mielke, Lisa A. [1 ]
O'Farrell, Laura K. [1 ]
Lavelle, Ed [1 ]
Mori, Andres [1 ]
McCarthy, Geraldine M. [2 ]
Mills, Kingston H. G. [1 ]
Dunne, Aisling [1 ]
机构
[1] Trinity Coll Dublin, Sch Biochem & Immunol, Immunol Res Ctr, Dublin 2, Ireland
[2] Mater Misericordiae Univ Hosp, Dept Rheumatol, Dublin 7, Ireland
基金
爱尔兰科学基金会;
关键词
Osteoarthritis; Inflammation; Tyrosine kinases; Danger molecules; Cytokines; NECROSIS-FACTOR-ALPHA; RHEUMATOID-ARTHRITIS; HUMAN FIBROBLASTS; MONOSODIUM URATE; INTERLEUKIN-1-BETA; HYDROXYAPATITE; PATHOGENESIS; MECHANISM;
D O I
10.1016/j.clim.2012.06.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The pro-inflammatory cytokines, TNF alpha, IL-1 and IL-18, amplify cartilage destruction associated with osteoarthritis (OA). Current data suggest that basic calcium phosphate (BCP) crystals are potent drivers of inflammatory mediator and matrix metalloprotease expression in the OA joint. It has previously been demonstrated that synovial macrophages play a role in initiating and driving BCP-induced inflammation. However, the molecular mechanisms by which BCP crystals exert their effects remain unclear. Here we demonstrate that exposure of macrophages to BCP crystals leads to activation of Syk and PI3 kinase. Furthermore, we show that production of pro-inflammatory cytokines and phosphorylation of the downstream kinase, ERK, are suppressed following treatment with Syk and PI3 kinase inhibitors. Finally, we demonstrate that treatment of macrophages with BCP crystals induces the production of the damage-associated molecule, S100A8, in a Syk dependent manner. We therefore identify Syk and PI3 kinase as potential novel targets for the treatment of BCP-related pathologies. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:228 / 236
页数:9
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