Department of Stem Cell Biology, Hagedorn Research Institute, Gentofte, Denmark.
Stem Cells Dev. 2011 Nov;20(11):1817-27. doi: 10.1089/scd.2011.0042. Epub 2011 Apr 6.
The homeobox gene Noto is expressed in the node and its derivative the notochord. Here we use a targeted Noto-GFP reporter to isolate and characterize node/notochord-like cells derived from mouse embryonic stem cells. We find very few Noto-expressing cells after spontaneous differentiation. However, the number of Noto-expressing cells was increased when using Activin A to induce a Foxa2- and Brachyury-expressing progenitor population, whose further differentiation into Noto-expressing cells was improved by simultaneous inhibition of BMP, Wnt, and retinoic acid signaling. Noto-GFP(+) cells expressed the node/notochord markers Noto, Foxa2, Shh, Noggin, Chordin, Foxj1, and Brachyury; showed a vacuolarization characteristic of notochord cells; and can integrate into midline structures when grafted into Hensen's node of gastrulating chicken embryos. The ability to generate node/notochord-like cells in vitro will aid the biochemical characterization of these developmentally important structures.
同源盒基因 Noto 表达于脊索中胚层原条及其衍生物脊索中。在这里,我们利用一个靶向的 Noto-GFP 报告基因来分离和鉴定由小鼠胚胎干细胞诱导而来的具有原条/脊索样特性的细胞。我们发现自发分化后仅有少量 Noto 表达的细胞。然而,当利用激活素 A 诱导 Foxa2 和 Brachyury 表达的前体细胞群时,Noto 表达的细胞数量增加,同时抑制 BMP、Wnt 和视黄酸信号通路则可以促进其向 Noto 表达细胞的分化。Noto-GFP(+)细胞表达了原条/脊索的标记物 Noto、Foxa2、Shh、Noggin、Chordin、Foxj1 和 Brachyury;呈现脊索细胞的空泡化特征;并且可以整合到鸡胚原条的中轴结构中。体外生成原条/脊索样细胞的能力将有助于对这些对发育非常重要的结构进行生化特征分析。