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Hes binding to STAT3 mediates crosstalk between Notch and JAK-STAT signalling.
Kamakura, Sachiko; Oishi, Koji; Yoshimatsu, Takeshi; Nakafuku, Masato; Masuyama, Norihisa; Gotoh, Yukiko.
Afiliação
  • Kamakura S; Institute of Molecular and Cellular Biosciences, University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.
Nat Cell Biol ; 6(6): 547-54, 2004 Jun.
Article em En | MEDLINE | ID: mdl-15156153
Although the Notch and JAK-STAT signalling pathways fulfill overlapping roles in growth and differentiation regulation, no coordination mechanism has been proposed to explain their relationship. Here we show that STAT3 is activated in the presence of active Notch, as well as the Notch effectors Hes1 and Hes5. Hes proteins associate with JAK2 and STAT3, and facilitate complex formation between JAK2 and STAT3, thus promoting STAT3 phosphorylation and activation. Furthermore, suppression of endogenous Hes1 expression reduces growth factor induction of STAT3 phosphorylation. STAT3 seems to be essential for maintenance of radial glial cells and differentiation of astrocytes by Notch in the developing central nervous system. These results suggest that direct protein-protein interactions coordinate cross-talk between the Notch-Hes and JAK-STAT pathways.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Fatores de Transcrição / Proteínas Tirosina Quinases / Transdução de Sinais / Transativadores / Proteínas Proto-Oncogênicas / Receptores de Superfície Celular / Proteínas de Homeodomínio / Proteínas de Ligação a DNA Limite: Animals Idioma: En Revista: Nat Cell Biol Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Japão
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Fatores de Transcrição / Proteínas Tirosina Quinases / Transdução de Sinais / Transativadores / Proteínas Proto-Oncogênicas / Receptores de Superfície Celular / Proteínas de Homeodomínio / Proteínas de Ligação a DNA Limite: Animals Idioma: En Revista: Nat Cell Biol Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Japão