Disease-specific proteins from rheumatoid arthritis patients

被引:33
|
作者
Kim, Choong Won
Cho, Eun Hye
Lee, Yun Jong
Kim, Yoon Hee
Hah, Young-Sool
Kim, Deok Ryong
机构
[1] Gyeongsang Natl Univ, Coll Med, Dept Biochem, Jinju 660751, South Korea
[2] Gyeongsang Natl Univ, Coll Med, RINS, Jinju 660751, South Korea
[3] Gyeongsang Natl Univ, Inst Hlth Sci, Jinju 660751, South Korea
[4] Seoul Natl Univ, Bundang Hosp, Dept Internal Med, Songnam, South Korea
关键词
arthritis; rheumatoid; autoantigens; fibronectins; proteomics;
D O I
10.3346/jkms.2006.21.3.478
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rheumatoid arthritis (RA) is a chronic inflammatiory disease that mainly destroys cartilages or bones at the joints. This inflammatory disorder is initiated by self-attack using own immune system, but the detail of pathological mechanism is unclear. Features of autoantigens leading to autoimmune disease are also under veil although several candidates including type II collagen have been suggested to play a role in pathogenesis. In this report, we tried to identify proteins responding to antibodies purified from RA patients and screen proteins up-regulated or down-regulated in RA using proteomic approach. Fibronectin, semaphorin 7A precursor, growth factor binding protein 7 (GRB7), and immunoglobulin mu chain were specifically associated with antibodies isolated from RA synovial fluids. In addition, some metabolic proteins such as adipocyte fatty acid binding protein, galectin-1 and apolipoprotein A1 precursor were overexpressed in RA synovium. Also, expression of peroxiredoxin 2 was up-regulated in RA. On the contrary, expression of vimentin was severely suppressed in RA synoviocytes. Such findings might give some insights into understanding of pathological mechanism in RA.
引用
收藏
页码:478 / 484
页数:7
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