Nigmatullina Lira, Norkin Maxim, Dzama Margarita M, Messner Berith, Sayols Sergi, Soshnikova Natalia
Institute of Molecular Biology, Mainz, Germany.
Institute of Molecular Biology, Mainz, Germany
EMBO J. 2017 Apr 3;36(7):869-885. doi: 10.15252/embj.201694959. Epub 2017 Jan 11.
The adult intestinal stem cells (ISCs), their hierarchies, mechanisms of maintenance and differentiation have been extensively studied. However, when and how ISCs are established during embryogenesis remains unknown. We show here that the transcription regulator Id2 controls the specification of embryonic Lgr5 progenitors in the developing murine small intestine. Cell fate mapping analysis revealed that Lgr5 progenitors emerge at E13.5 in wild-type embryos and differ from the rest on the intestinal epithelium by a characteristic ISC signature. In the absence of Id2, the intestinal epithelium differentiates into Lgr5 cells already at E9.5. Furthermore, the size of the Lgr5 cell pool is significantly increased. We show that Id2 restricts the activity of the Wnt signalling pathway at early stages and prevents precocious differentiation of the embryonic intestinal epithelium. Id2-deficient embryonic epithelial cells cultured strongly activate Wnt target genes as well as markers of neoplastic transformation and form fast growing undifferentiated spheroids. Furthermore, adult ISCs from Id2-deficient mice display a distinct transcriptional signature, supporting an essential role for Id2 in the correct specification of ISCs.
成体肠干细胞(ISC)及其层级结构、维持和分化机制已得到广泛研究。然而,ISC在胚胎发育过程中何时以及如何形成仍不清楚。我们在此表明,转录调节因子Id2控制发育中小鼠小肠中胚胎Lgr5祖细胞的特化。细胞命运图谱分析显示,Lgr5祖细胞在野生型胚胎的E13.5出现,并通过特征性的ISC标记与肠道上皮的其他细胞不同。在没有Id2的情况下,肠道上皮在E9.5就已分化为Lgr5细胞。此外,Lgr5细胞池的大小显著增加。我们表明,Id2在早期阶段限制Wnt信号通路的活性,并防止胚胎肠道上皮过早分化。培养的Id2缺陷胚胎上皮细胞强烈激活Wnt靶基因以及肿瘤转化标记,并形成快速生长的未分化球体。此外,来自Id2缺陷小鼠的成体ISC表现出独特的转录特征,支持Id2在ISC正确特化中的重要作用。