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成纤维细胞生长因子(FGF)通过PI 3-激酶和Akt/PKB的信号传导是胚状体分化所必需的。

Fibroblast growth factor (FGF) signaling through PI 3-kinase and Akt/PKB is required for embryoid body differentiation.

作者信息

Chen Y, Li X, Eswarakumar V P, Seger R, Lonai P

机构信息

Department of Molecular Genetics, The Weizmann Institute of Science, Rehovot, Israel.

出版信息

Oncogene. 2000 Aug 3;19(33):3750-6. doi: 10.1038/sj.onc.1203726.

Abstract

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 PLCgamma-1, as compared to the wild type, while the activation of MAPK/Erk was less affected. Requirement for PI 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.

摘要

在胚胎干细胞来源的胚状体中研究了成纤维细胞生长因子(FGF)信号传导在早期上皮分化中的作用。通过将在其酶结构域中截短的Fgfr2 cDNA稳定导入胚胎干细胞,产生了一种显性负性成纤维细胞生长因子受体(FGFR)突变体。这些细胞无法分化为囊性胚状体。在突变体中,尽管其细胞增殖速率保持不变,但未观察到上皮分化和空化形态发生。与野生型相比,该表型与Akt/PKB和PLCγ-1的激活显著降低有关,而MAPK/Erk的激活受影响较小。特异性抑制剂证明了胚状体分化中对PI 3-激酶信号传导的需求。在短期实验中,渥曼青霉素消除了Akt/PKB的激活。在长期培养中,Ly294002抑制胚胎干细胞向胚状体的分化。我们的数据表明,对于早期上皮分化,FGF信号传导需要通过PI 3-激酶-Akt/PKB途径。

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