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Published on: September 15, 2017
Temporal expression of growth factors triggered by epiregulin regulates inflammation development
Masaya Harada1, Daisuke Kamimura1, Yasunobu Arima1
1Division of Molecular Neuroimmunology, Institute for Genetic Medicine and Graduate School of Medicine, Hokkaido University, Sapporo 060-0815, Japan; Laboratory of Developmental Immunology, Japan Science and Technology Agency-Core Research for Engineering, Science, and Technology, Graduate School of Frontier Biosciences, Osaka University, Osaka 565-0871, Japan; Laboratory of Developmental Immunology, Japan Science and Technology Agency-Core Research for Engineering, Science, and Technology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan; Laboratory of Developmental Immunology, Japan Science and Technology Agency-Core Research for Engineering, Science, and Technology, World Premier International Immunology Frontier Research Center, Osaka University, Osaka 565-0871, Japan;
Abstract:
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.
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