Crawford T Quinn, Roelink Henk
Department of Biological Structure, University of Washington School of Medicine, Seattle, WA 98195-7420, USA.
Dev Dyn. 2007 Mar;236(3):886-92. doi: 10.1002/dvdy.21083.
During development of the neural tube, inhibition of the Notch response as well as the activation of the Sonic Hedgehog (Shh) response results in the formation of neuronal cell types. To determine whether Shh and Notch act independently, we tested the effects of the Notch inhibitor DAPT (N-[N-(3,5-difluorophenacetyl)-l-alanyl]-S-phenylglycine t-butyl ester) on neuralized, embryonic stem (ES) cell-derived embryoid bodies (EBs), while varying the levels of Shh pathway activation. Shh-resistant EBs were derived from Smo null ES cells, while EBs with constitutive high level of Shh pathway activation were derived from Ptc1 null ES cells. Intermediate levels of Shh pathway activation was achieved by the addition of ShhN to the EB culture medium. It was found that DAPT-mediated inhibition of the Notch response resulted in enhanced neuronal differentiation. In the absence of Shh, more interneurons were detected, while the main effect of DAPT on EBs with an activated Shh response was the precocious loss of ventral neuronal precursor-specific markers.
在神经管发育过程中,Notch反应的抑制以及音猬因子(Shh)反应的激活会导致神经元细胞类型的形成。为了确定Shh和Notch是否独立发挥作用,我们测试了Notch抑制剂DAPT(N-[N-(3,5-二氟苯乙酰基)-L-丙氨酰基]-S-苯甘氨酸叔丁酯)对经神经诱导的、胚胎干细胞(ES)来源的胚状体(EB)的影响,同时改变Shh信号通路的激活水平。抗Shh的EB来自Smo基因缺失的ES细胞,而具有组成性高水平Shh信号通路激活的EB来自Ptc1基因缺失的ES细胞。通过向EB培养基中添加ShhN来实现Shh信号通路激活的中间水平。结果发现,DAPT介导的Notch反应抑制导致神经元分化增强。在没有Shh的情况下,检测到更多的中间神经元,而DAPT对具有激活的Shh反应的EB的主要作用是腹侧神经元前体特异性标志物的过早丢失。