Temporal Expression of Growth Factors Triggered by Epiregulin Regulates Inflammation Development

被引:55
作者
Harada, Masaya [1 ,2 ,3 ,4 ,5 ]
Kamimura, Daisuke [1 ,2 ,3 ,4 ,5 ]
Arima, Yasunobu [1 ,2 ,3 ,4 ,5 ]
Kohsaka, Hitoshi [6 ]
Nakatsuji, Yuji [7 ]
Nishida, Makoto [8 ]
Atsumi, Toru [1 ,2 ,3 ,4 ,5 ]
Meng, Jie [1 ,2 ,3 ,4 ,5 ]
Bando, Hidenori [1 ,2 ,3 ,4 ,5 ]
Singh, Rajeev [1 ,2 ]
Sabharwal, Lavannya [1 ,2 ,3 ,4 ,5 ]
Jiang, Jing-Jing [1 ,2 ,3 ,4 ,5 ]
Kumai, Noriko [1 ,2 ,3 ,4 ,5 ]
Miyasaka, Nobuyuki [6 ]
Sakoda, Saburo [9 ]
Yamauchi-Takihara, Keiko [5 ,8 ]
Ogura, Hideki [1 ,2 ,3 ,4 ]
Hirano, Toshio [10 ]
Murakami, Masaaki [1 ,2 ,3 ,4 ,5 ]
机构
[1] Hokkaido Univ, Div Mol Neuroimmunol, Inst Med Genet, Sapporo, Hokkaido 0600815, Japan
[2] Hokkaido Univ, Grad Sch Med, Sapporo, Hokkaido 0600815, Japan
[3] Osaka Univ, Lab Dev Immunol, Japan Sci & Technol Agcy, Core Res Engn Sci & Technol,Grad Sch Frontier Bio, Osaka 5650871, Japan
[4] Osaka Univ, Japan Sci & Technol Agcy, Core Res Engn Sci & Technol, Lab Dev Immunol,Grad Sch Med, Osaka 5650871, Japan
[5] Osaka Univ, Japan Sci & Technol Agcy, World Premier Int Immunol Frontier Res Ctr, Lab Dev Immunol,Core Res Engn Sci & Technol, Osaka 5650871, Japan
[6] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Med & Rheumatol, Tokyo 1138519, Japan
[7] Osaka Univ, Grad Sch Med, Dept Neurol, Osaka 5650871, Japan
[8] Osaka Univ, Hlth Care Ctr, Osaka 5600043, Japan
[9] Toneyama Hosp, Natl Hosp Org, Dept Neurol, Osaka 5600045, Japan
[10] Osaka Univ, Core Res Engn Sci & Technol, Japan Sci & Technol Agcy, Osaka, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
T-CELLS; AUTOIMMUNE ARTHRITIS; POSITIVE-FEEDBACK; IL-6; AMPLIFIER; IN-VIVO; INTERLEUKIN-6; GP130; ACTIVATION; RESPONSES; BETA;
D O I
10.4049/jimmunol.1400562
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this study, we investigated the relationship between several growth factors and inflammation development. Serum concentrations of epiregulin, amphiregulin, betacellulin, TGF-alpha, fibroblast growth factor 2, placental growth factor (PLGF), and tenascin C were increased in rheumatoid arthritis patients. Furthermore, local blockades of these growth factors suppressed the development of cytokine-induced arthritis in mice by inhibiting chemokine and IL-6 expressions. We found that epiregulin expression was early and followed by the induction of other growth factors at different sites of the joints. The same growth factors then regulated the expression of epiregulin at later time points of the arthritis. These growth factors were increased in patients suffering from multiple sclerosis (MS) and also played a role in the development of an MS model, experimental autoimmune encephalomyelitis. The results suggest that the temporal expression of growth factors is involved in the inflammation development seen in several diseases, including rheumatoid arthritis and MS. Therefore, various growth factor pathways might be good therapeutic targets for various inflammatory diseases.
引用
收藏
页码:1039 / 1046
页数:8
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