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Fibroblast growth factor (FGF) signaling through PI 3-kinase and Akt/PKB is required for embryoid body differentiation
被引:104
|作者:
Chen, Y
Li, XF
Eswarakumar, VP
Seger, R
Lonai, P
[1
]
机构:
[1] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Regulat Biol, IL-76100 Rehovot, Israel
来源:
关键词:
embryoid bodies;
FGF signaling;
epithelial differentiation;
Akt/PKB;
PLC gamma-1;
D O I:
10.1038/sj.onc.1203726
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The role of FGF signaling in early epithelial differentiation was investigated in ES (embryonic) stem) cell derived embryoid bodies. A dominant negative fibroblast growth factor receptor (FGFR) mutation was created by stably introducing into ES cells an Fgfr2 cDNA, truncated in its enzymatic domains. These cells failed to differentiate into cystic embryoid bodies. No epithelial differentiation and cavitation morphogenesis could be observed, in the mutant, although its rate of cell proliferation remained unchanged. This phenotype was associated with a significant decrease in the activation of Akt/PKB and PLC gamma-1, as compared to the wild type, while the activation of MAPK/Erk was less affected, Requirement for PL 3-kinase signaling in embryoid body differentiation was demonstrated by specific inhibitors, Akt/PKB activation was abrogated by wortmannin in short-term experiments. In long-term cultures Ly294002 inhibited the differentiation of ES cells into embryoid bodies. Our data demonstrate that for early epithelial differentiation FGF signaling is required through the PI 3-kinase-Akt/ PKB pathway.
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页码:3750 / 3756
页数:7
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