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Temporal expression of growth factors triggered by epiregulin regulates inflammation development.
Harada, Masaya; Kamimura, Daisuke; Arima, Yasunobu; Kohsaka, Hitoshi; Nakatsuji, Yuji; Nishida, Makoto; Atsumi, Toru; Meng, Jie; Bando, Hidenori; Singh, Rajeev; Sabharwal, Lavannya; Jiang, Jing-Jing; Kumai, Noriko; Miyasaka, Nobuyuki; Sakoda, Saburo; Yamauchi-Takihara, Keiko; Ogura, Hideki; Hirano, Toshio; Murakami, Masaaki.
Afiliación
  • Harada M; Division 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
  • Kamimura D; Division 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
  • Arima Y; Division 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
  • Kohsaka H; Department of Medicine and Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8519, Japan;
  • Nakatsuji Y; Department of Neurology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan;
  • Nishida M; Health Care Center, Osaka University, Osaka 560-0043, Japan;
  • Atsumi T; Division 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
  • Meng J; Division 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
  • Bando H; Division 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
  • Singh R; Division of Molecular Neuroimmunology, Institute for Genetic Medicine and Graduate School of Medicine, Hokkaido University, Sapporo 060-0815, Japan;
  • Sabharwal L; Division 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
  • Jiang JJ; Division 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
  • Kumai N; Division 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
  • Miyasaka N; Department of Medicine and Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8519, Japan;
  • Sakoda S; Department of Neurology, National Hospital Organization Toneyama Hospital, Osaka 560-0045, Japan; and.
  • Yamauchi-Takihara K; Health Care Center, Osaka University, Osaka 560-0043, Japan;
  • Ogura H; Division 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
  • Hirano T; Japan Science and Technology Agency-Core Research for Engineering, Science, and Technology, Osaka University, 565-0871, Japan.
  • Murakami M; Division 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
J Immunol ; 194(3): 1039-46, 2015 Feb 01.
Article en En | MEDLINE | ID: mdl-25556244
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.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Regulación de la Expresión Génica / Péptidos y Proteínas de Señalización Intercelular / Epirregulina / Inflamación Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Immunol Año: 2015 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Regulación de la Expresión Génica / Péptidos y Proteínas de Señalización Intercelular / Epirregulina / Inflamación Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Immunol Año: 2015 Tipo del documento: Article