FGF signaling mediates definitive endoderm formation by regulating epithelial-to-mesenchymal transition and cell proliferation

被引:5
|
作者
Li, Shengbiao [1 ,3 ]
Huang, Qingsong [2 ]
Mao, Jianwen [2 ]
Li, Qiuhong [1 ,2 ]
机构
[1] Southwest Med Univ, Sch Basic Med Sci, Luzhou, Peoples R China
[2] Guangdong Pharmaceut Univ, Guangdong Prov Key Lab Pharmaceut Bioact Subst, Guangzhou, Peoples R China
[3] Chinese Acad Sci, South China Inst Stem Cell Biol & Regenerat Med, Guangzhou Inst Biomed & Hlth, Guangzhou, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
definitive endoderm; FGF signaling; EMT; cell proliferation; MORPHOGENETIC MOVEMENT; STEM-CELLS; GROWTH; DIFFERENTIATION; INDUCTION;
D O I
10.1387/ijdb.190372ql
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
FGF signaling pathway is imperative for definitive endoderm (DE) differentiation from human embryonic stem cells (hESCs), which always accompanies an epithelial-to-mesenchymal transition (EMT) process. However, whether there is an association between FGF signaling and the EMT during DE formation in vitro has remained elusive. In the present study, we identify that several FGF family members were significantly activated during the differentiation of hESCs toward DE. Inhibition of FGF signaling by an efficient and selective inhibitor BGJ398 abolishes both the EMT and DE induction by blocking the activation of the zinc-finger transcription factor SNAI1 which is a direct transcriptional repressor of cell adhesion protein CDH1. In addition, cell proliferation is also severely influenced by attenuating the FGF signaling. Collectively, we propose that the FGF signaling promotes the DE formation through mediating the EMT and cell proliferation.
引用
收藏
页码:471 / 477
页数:7
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