Anteriorization of neural fate by inhibitor of β-catenin and T cell factor (ICAT), a negative regulator of Wnt signaling

被引:49
|
作者
Satoh, K
Kasai, M
Ishidao, T
Tago, K
Ohwada, S
Hasegawa, Y
Senda, T
Takada, S
Nada, S
Nakamura, T
Akiyama, T
机构
[1] Univ Tokyo, Lab Mol & Genet Informat, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[2] Gunma Univ, Grad Sch Med, Dept Surg, Maebashi, Gumma 3718511, Japan
[3] Fujita Hlth Univ, Dept Anat 1, Sch Med, Aichi 4701192, Japan
[4] Kyoto Univ, Ctr Mol & Dev Biol, Grad Sch Sci, Sakyo Ku, Kyoto 6068502, Japan
[5] Osaka Univ, Dept Oncogene Res, Res Inst Microbial Dis, Suita, Osaka 5650871, Japan
关键词
D O I
10.1073/pnas.0401733101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Inhibitor of beta-catenin and T cell factor (ICAT) inhibits Wnt signaling by interfering with the interaction between beta-catenin and T cell factor. Here we show that ICAT(-/-) embryos exhibit malformation of the forebrain and craniofacial bones and lack the kidney. Analysis of the neuronal differentiation of embryonic stem cells revealed that Wnt3a redirects the fate of neural progenitors to a posterior character, whereas ICAT induces forebrain cells by inhibiting Wnt signaling. Furthermore, ICAT(-/-) embryonic stem cells were found to differentiate into neuronal cells possessing a posterior character. These results suggest that ICAT plays an important role in the anteriorization of neural cells by inhibiting the posteriorizing activity of Wnt signaling.
引用
收藏
页码:8017 / 8021
页数:5
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