Center for Cancer and Stem Cell Biology, Institute of Biosciences and Technology, Texas A&M Health Science Center, Houston, TX, USA.
Autophagy. 2012 Apr;8(4):690-1. doi: 10.4161/auto.19290. Epub 2012 Apr 1.
The fibroblast growth factor (FGF) signaling axis plays important roles in heart development. Yet, the molecular mechanism by which the FGF regulates cardiogenesis is not fully understood. Using genetically engineered mouse and in vitro cultured embryoid body (EB) models, we demonstrate that FGF signaling suppresses premature differentiation of heart progenitor cells, as well as autophagy in outflow tract (OFT) myocardiac cells. The FGF also promotes mesoderm differentiation in embryonic stem cells (ESCs) but inhibits cardiomyocyte differentiation of the mesoderm cells at later stages. Furthermore, inhibition of FGF signaling increases myocardial differentiation and autophagy in both ex vivo cultured embryos and EBs, whereas activation of autophagy promotes myocardial differentiation. Thus, a link between FGF signals preventing premature differentiation of heart progenitor cells and suppression of autophagy has been established. These findings provide the first evidence that autophagy plays a role in heart progenitor differentiation, and suggest a new venue to regulate stem/progenitor cell differentiation.
成纤维细胞生长因子 (FGF) 信号轴在心脏发育中发挥重要作用。然而,FGF 调节心脏发生的分子机制尚不完全清楚。我们使用基因工程小鼠和体外培养的类胚体 (EB) 模型,证明 FGF 信号抑制心脏祖细胞的过早分化,以及流出道 (OFT) 心肌细胞的自噬。FGF 还促进胚胎干细胞 (ESCs) 中的中胚层分化,但在后期阶段抑制中胚层细胞向心肌细胞分化。此外,抑制 FGF 信号会增加体外培养胚胎和 EB 中的心肌分化和自噬,而激活自噬会促进心肌分化。因此,已经建立了 FGF 信号防止心脏祖细胞过早分化和抑制自噬之间的联系。这些发现提供了自噬在心脏祖细胞分化中起作用的第一个证据,并为调节干细胞/祖细胞分化提供了一个新的途径。