Chen Ming, Qian Cheng, Bi Lin-Lin, Zhao Fang, Zhang Guang-Yu, Wang Zhi-Quan, Gan Xue-Dong, Wang Yang-Gan
Department of Cardiology, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China,
Biotechnol Lett. 2015 Feb;37(2):475-81. doi: 10.1007/s10529-014-1700-5. Epub 2014 Oct 14.
Embryoid bodies (EBs) with large starting numbers of embryonic stem cells (ESCs) have a greater degree of cardiac differentiation than from low numbers of EBs. However, the biological roles of signaling molecules in these effects are not well understood. Here, we show that groups of EBs with different starting numbers of ESCs had differential gene expression patterns for Wnt5a and Wnt11. Wnt11 significantly increased the percentage of beating EBs by up-regulating the expression of the cardiac-specific genes. Wnt5a did not show these effects. Moreover, Wnt11 significantly increased the level of phosphorylated Jun N-terminal kinase. The inhibition of the JNK pathway by SP600125 blocked the effects of Wnt11. Thus, enrichment of cardiac differentiation in groups of EBs with a larger starting number of ESCs is mediated by the Wnt11-JNK pathway.
起始胚胎干细胞(ESC)数量较多的胚状体(EB)比数量较少的EB具有更高程度的心脏分化。然而,信号分子在这些效应中的生物学作用尚未得到充分理解。在此,我们表明,具有不同起始ESC数量的EB组在Wnt5a和Wnt11的基因表达模式上存在差异。Wnt11通过上调心脏特异性基因的表达显著增加了跳动EB的百分比。Wnt5a未显示出这些效应。此外,Wnt11显著增加了磷酸化的Jun N末端激酶的水平。SP600125对JNK通路的抑制阻断了Wnt11的效应。因此,起始ESC数量较多的EB组中心脏分化的富集是由Wnt11-JNK通路介导的。