Notch Signaling Mediates TNF-α-Induced IL-6 Production in Cultured Fibroblast-Like Synoviocytes from Rheumatoid Arthritis

被引:43
|
作者
Jiao, Zhijun [1 ,2 ]
Wang, Wenhong [3 ]
Ma, Jie [4 ]
Wang, Shengjun [4 ]
Su, Zhaoliang [4 ]
Xu, Huaxi [4 ]
机构
[1] Jiangsu Univ, Affiliated Hosp, Key Lab Med Immunol, Zhenjiang 212001, Peoples R China
[2] Jiangsu Univ, Affiliated Hosp, Dept Lab Med, Zhenjiang 212001, Peoples R China
[3] Jiangsu Univ, Sch Med Sci & Lab Med, Dept Pathogen Biol, Zhenjiang 212013, Peoples R China
[4] Jiangsu Univ, Sch Med Sci & Lab Med, Dept Immunol, Zhenjiang 212013, Peoples R China
关键词
CLASSIFICATION; OSTEOARTHRITIS; EXPRESSION; CRITERIA; CELLS;
D O I
10.1155/2012/350209
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It has been reported that Notch family proteins are expressed in synovium tissue and involved in the proliferation of synoviocyte from rheumatoid arthritis (RA). The aim of this paper was to investigate whether Notch signaling mediated TNF-alpha-induced cytokine production of cultured fibroblast-like synoviocytes (FLSs) from RA. Exposure of RA FLSs to TNF-alpha (10 ng/ml) led to increase of Hes-1, a target gene of Notch signaling, and a marked upregulation of Notch 2, Delta-like 1, and Delta-like 3 mRNA levels. Blockage of Notch signaling by a.-secretase inhibitor (DAPT) inhibited IL-6 secretion of RA FLSs in response to TNF-alpha while treatment with recombinant fusion protein of Notch ligand Delta-like 1 promoted such response. TNF-alpha stimulation also induced IL-6 secretion in OA FLSs; however, the Hes-1 level remained unaffected. Our data confirm the functional involvement of Notch pathway in the pathophysiology of RA FLSs which may provide a new target for RA therapy.
引用
收藏
页数:6
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