Stringer Emma J, Pritchard Catrin A, Beck Felix
Department of Biochemistry, University of Leicester, Leicester, UK.
FEBS Lett. 2008 Jul 23;582(17):2555-60. doi: 10.1016/j.febslet.2008.06.024. Epub 2008 Jun 23.
Null mutation or haploinsufficiency of Cdx2 results in the development of heterotopic lesions with a gastric phenotype in the midgut endoderm. Conversely transgenic expression of Cdx2 in the stomach causes the endoderm to differentiate into intestinal-type mucosa. We demonstrate that the mesoderm adjacent to intestinal heterotopic areas expresses stomach specific Barx1 while the surrounding mesoderm is Barx1 negative. We conclude that the initiation of gut histodifferentiation lies in the endodermal expression of Cdx2 and that endodermal/mesodermal cross-talk involving Barx1 with appropriate feedback loops results in the development of the postnatal gut phenotype.
Cdx2的无效突变或单倍剂量不足会导致中肠内胚层出现具有胃表型的异位病变。相反,在胃中Cdx2的转基因表达会使内胚层分化为肠型黏膜。我们证明,与肠道异位区域相邻的中胚层表达胃特异性的Barx1,而周围的中胚层Barx1呈阴性。我们得出结论,肠道组织分化的起始在于Cdx2在内胚层的表达,并且涉及Barx1的内胚层/中胚层相互作用以及适当的反馈环导致了出生后肠道表型的发育。