Brigham and Women's Hospital and Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.
Mech Dev. 2011 Sep-Dec;128(7-10):387-400. doi: 10.1016/j.mod.2011.07.005. Epub 2011 Aug 10.
Wnt signaling has been implicated in many developmental processes, but its role in early endoderm development is not well understood. Wnt signaling is active in posterior endoderm as early as E7.5. Genetic and chemical activation show that the Wnt pathway acts directly on endoderm to induce the intestinal master regulator Cdx2, shifting global gene away from anterior endoderm and toward a posterior, intestinal program. In a mouse embryonic stem cell differentiation platform that yields pure populations of definitive endoderm, Wnt signaling induces intestinal gene expression in all cells. We have identified a set of genes specific to the anterior small intestine, posterior small intestine, and large intestine during early development, and show that Wnt, through Cdx2, activates large intestinal gene expression at high doses and small intestinal gene expression at lower doses. These findings shed light on the mechanism of embryonic intestinal induction and provide a method to manipulate intestinal development from embryonic stem cells.
Wnt 信号通路在许多发育过程中都有涉及,但它在早期内胚层发育中的作用还不是很清楚。Wnt 信号通路在 E7.5 时就已经在后端内胚层中活跃。遗传和化学激活表明,Wnt 途径直接作用于内胚层,诱导肠道主调控因子 Cdx2 的表达,使全局基因从前端内胚层向后端、向肠道程序转移。在一个能够产生纯系定型内胚层的小鼠胚胎干细胞分化平台中,Wnt 信号通路诱导所有细胞中肠道基因的表达。我们鉴定了一组在早期发育过程中特异性表达于前小肠、后小肠和大肠的基因,并表明 Wnt 通过 Cdx2 在高剂量时激活大肠基因的表达,在低剂量时激活小肠基因的表达。这些发现揭示了胚胎肠道诱导的机制,并提供了一种从胚胎干细胞中操纵肠道发育的方法。