CTRP3 plays an important role in the development of collagen-induced arthritis in mice

被引:70
|
作者
Murayama, Masanori A. [1 ,2 ,3 ]
Kakuta, Shigeru [1 ]
Maruhashi, Takumi [1 ]
Shimizu, Kenji [1 ]
Seno, Akimasa [1 ,2 ]
Kubo, Sachiko [1 ]
Sato, Nozomi [1 ]
Saijo, Shinobu [1 ,4 ]
Hattori, Masahira [2 ]
Iwakura, Yoichiro [1 ,2 ,3 ]
机构
[1] Univ Tokyo IMSUT, Inst Med Sci, Ctr Expt Med & Syst Biol, Tokyo 1088639, Japan
[2] Univ Tokyo, Grad Sch Frontier Sci, Dept Computat Biol, Kashiwa, Chiba 2770882, Japan
[3] Japan Sci & Technol Agcy JST, Core Res Evolut Sci & Technol, Kawaguchi, Saitama 3320012, Japan
[4] JST, PRESTO, Kawaguchi, Saitama 3320012, Japan
关键词
Rheumatoid arthritis; Collagen-induced arthritis; CTRP3; RESEMBLING RHEUMATOID-ARTHRITIS; ADIPOSE-TISSUE; COMPLEMENT; ADIPONECTIN; ANTAGONIST; DEFICIENT; INDUCTION; PROTOCOL; PARALOG; PATHWAY;
D O I
10.1016/j.bbrc.2013.11.040
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
Rheumatoid arthritis (RA) is an autoimmune inflammatory disease exhibited most commonly in joints. We found that the expression of C1qtnf3, which encodes C1q/TNF-related protein 3 (CTRP3), was highly increased in two mouse RA models with different etiology. To elucidate the pathogenic roles of CTRP3 in the development of arthritis, we generated C1qtnf3(-/-) mice and examined the development of collagen-induced arthritis in these mice. We found that the incidence and severity score was higher in C1qtnf3(-/-) mice compared with wild-type (WT) mice. Histopathology of the joints was also more severe in C1qtnf3(-/-) mice. The levels of antibodies against type II collagen and pro-inflammatory cytokine mRNAs in C1qtnf3(-/-) mice were higher than WT mice. These observations indicate that CTRP3 plays an important role in the development of autoimmune arthritis, suggesting CTRP3 as a possible medicine to treat RA. (C) 2013 The Authors. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:42 / 48
页数:7
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