Activation of Stat3 by cytokine receptor gp130 ventralizes Xenopus embryos independent of BMP-4

被引:26
|
作者
Nishinakamura, R
Matsumoto, Y
Matsuda, T
Ariizumi, T
Heike, T
Asashima, M
Yokota, T
机构
[1] Univ Tokyo, Inst Med Sci, Dept Stem Cell Regulat, Tokyo 1088639, Japan
[2] Tokai Univ, Dept Life Sci, Tokyo 1538902, Japan
关键词
gp130; Stat3; Smad2; Xenopus;
D O I
10.1006/dbio.1999.9518
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Stat3 is one of the main signaling components of cytokine receptors, including gp130. Here we show that activation of cytokine receptor gp130 resulted in a dramatic ventralization of Xenopus embryos and that the ventralization correlated well with Stat3 activation potential of the receptor. This finding led to identification of Xenopus Stat3 (Xstat3), which showed a 95% homology to its murine and human counterparts, at the amino acid level, and was expressed from the one-cell stage throughout development. The mechanism of gp130/XStat3-mediated ventralization proved to be independent of BMP-4. gp130/Xstat3 stimulation inhibited Smad2-induced ectopic axis formation in embryos and Smad2-dependent luciferase activity. A dominant-negative Stat3, in contrast, dorsalized Xenopus embryos, resulting in ectopic axis formation. We propose that Stat3-mediated signaling has the capacity to modify dorsoventral patterning in the early development of Xenopus. (C) 1999 Academic Press.
引用
收藏
页码:481 / 490
页数:10
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