Hes binding to STAT3 mediates crosstalk between Notch and JAK-STAT signalling

被引:345
|
作者
Kamakura, S
Oishi, K
Yoshimatsu, T
Nakafuku, M
Masuyama, N
Gotoh, Y
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[2] Cincinnati Childrens Hosp Res Fdn, Div Dev Biol, Cincinnati, OH 45229 USA
[3] Japan Sci & Technol Corp, PRESTO Project, Tokyo, Japan
[4] Japan Sci & Technol Corp, CREST Project, Tokyo, Japan
[5] Natl Inst Physiol Sci, Okazaki, Aichi 4448585, Japan
关键词
D O I
10.1038/ncb1138
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:547 / 554
页数:8
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