TY - JOUR
T1 - Temporal expression of growth factors triggered by epiregulin regulates inflammation development
AU - Harada, Masaya
AU - Kamimura, Daisuke
AU - Arima, Yasunobu
AU - Kohsaka, Hitoshi
AU - Nakatsuji, Yuji
AU - Nishida, Makoto
AU - Atsumi, Toru
AU - Meng, Jie
AU - Bando, Hidenori
AU - Singh, Rajeev
AU - Sabharwal, Lavannya
AU - Jiang, Jing Jing
AU - Kumai, Noriko
AU - Miyasaka, Nobuyuki
AU - Sakoda, Saburo
AU - Yamauchi-Takihara, Keiko
AU - Ogura, Hideki
AU - Hirano, Toshio
AU - Murakami, Masaaki
N1 - Publisher Copyright:
Copyright © 2015 by The American Association of Immunologists, Inc.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - In this study, we investigated the relationship between several growth factors and inflammation development. Serum concentrations of epiregulin, amphiregulin, betacellulin, TGF-α, 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.
AB - In this study, we investigated the relationship between several growth factors and inflammation development. Serum concentrations of epiregulin, amphiregulin, betacellulin, TGF-α, 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.
UR - http://www.scopus.com/inward/record.url?scp=84921493546&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.1400562
DO - 10.4049/jimmunol.1400562
M3 - 学術論文
C2 - 25556244
AN - SCOPUS:84921493546
SN - 0022-1767
VL - 194
SP - 1039
EP - 1046
JO - Journal of Immunology
JF - Journal of Immunology
IS - 3
ER -