Genetic mosaic analysis reveals that GATA-4 is required for proper differentiation of mouse gastric epithelium

被引:64
作者
Jacobsen, CM
Narita, N
Bielinska, M
Syder, AJ
Gordon, JI
Wilson, DB [1 ]
机构
[1] Washington Univ, Sch Med, Childrens Hosp, Dept Pediat, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Childrens Hosp, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[3] Univ Tsukuba, Dept Anat & Neurobiol, Tsukuba, Ibaraki 305, Japan
关键词
endoderm; stomach; transcription factor; H+; K+-ATPase; sonic hedgehog;
D O I
10.1006/dbio.2001.0424
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
During mouse embryogenesis GATA-4 is expressed first in primitive endoderm and then in definitive endoderm derivatives, including glandular stomach and intestine. To explore the role of GATA-4 in specification of definitive gastric endoderm, we generated chimeric mice by introducing Gata4(-/-) ES cells into ROSA26 morulae or blastocysts. In E14.5 chimeras, Gata4(-/-) cells were represented in endoderm lining the proximal and distal stomach. These cells expressed early cytodifferentiation markers, including GATA-6 and ApoJ. However, by E18.5, only rare patches of Gata4(-/-) epithelium were evident in the distal stomach. This heterotypic epithelium had a squamous morphology and did not express markers associated with differentiation of gastric epithelial cell lineages. Sonic Hedgehog, an endoderm-derived signaling molecule normally down-regulated in the distal stomach, was overexpressed in Gata4(-/-) cells. We conclude that GATA-4-deficient cells have an intrinsic defect in their ability to differentiate. Similarities in the phenotypes of Gata4(-/-) chimeras and mice with other genetically engineered mutations that affect gut development suggest that GATA-4 may be involved in the gastric epithelial response to members of the TGF-beta superfamily. (C) 2001 Elsevier Science.
引用
收藏
页码:34 / 46
页数:13
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