Expression of IL-17 homologs and their receptors in the synovial cells of rheumatoid arthritis patients

被引:2
|
作者
Hwang, SY [1 ]
Kim, HY
机构
[1] Hankyong Natl Univ, Inst Genet Engn, Grad Sch Biol & Informat Technol, Ansung 456749, South Korea
[2] Catholic Univ, Ctr Rheumatism Res, Seoul 137701, South Korea
关键词
fibroblast-like synoviocytes (FLS); interleukin-17; rheumatoid arthritis; synovial fluid mononuclear cell (SFMC);
D O I
暂无
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
IL-17 is a major proinflammatory cytokine secreted by activated T-lymphocytes that accumulates in the inflamed joints of rheumatoid arthritis (RA) patients. Additional IL-17-related molecules and their receptors have been discovered and may also contribute to RA pathogenesis. We examined the expression of the prototypic IL-17 (IL-17A) and its homologs, IL-17B-F, by RT-PCR analyses of synovial fluid mononuclear cells (SFMCs) and peripheral blood mononuclear cells (PBMCs) from RA patients. We also tested for induction of the IL-17 receptor homologs upon stimulation of the fibroblast-like synoviocytes (FLSs) of RA patients with IL-17. The patients' SFMCs expressed IL-17C, E and F in addition to IL-17A. As in the case of IL-17, IL-15 appears to be the major inducer of these homologs in RA SFMCs. We detected transcripts of IL-17R, as well as those of IL-17RB, C and D, in the FLSs of RA patients. Whereas IL-17R expression increased upon in vitro stimulation with IL-17, expression of IL-17RB, C and D was unchanged. However the possibility of cross-interaction between other IL-17 homologs and receptor isoforms remains to be investigated. Our data suggest that these additional homologs should also be considered as targets for immune modulation in the treatment of RA joint inflammation.
引用
收藏
页码:180 / 184
页数:5
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