Branching and differentiation defects in pulmonary epithelium with elevated Gata6 expression

被引:27
|
作者
Koutsourakis, M
Keijzer, R
Visser, P
Post, M
Tibboel, D
Grosveld, F
机构
[1] Erasmus Univ, Med Ctr, Dept Cell Biol & Genet, NL-3000 DR Rotterdam, Netherlands
[2] Sophia Childrens Hosp, Dept Pediat Surg, Rotterdam, Netherlands
[3] Univ Toronto, Hosp Sick Children, Res Inst, Lung Biol Res Program, Toronto, ON M5G 1X8, Canada
关键词
Gata6; overexpression; differentiation; branching; distal pulmonary epithelium;
D O I
10.1016/S0925-4773(01)00386-0
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The transcription factor GATA6 is expressed in the fetal pulmonary epithelium of the developing mouse lung and loss of function studies strongly suggested that it is required for proper branching morphogenesis and epithelial differentiation. We have further investigated the role of GATA6 in this process by utilizing a pulmonary epithelium specific promoter to maintain high levels of GATA6 protein during fetal lung development. Transgenic mice expressing Gata6 cDNA under the control of the human Surfactant Protein-C (SP-C) promoter were generated and their lungs were analyzed during fetal stages. Transgenic lungs exhibit branching defects as early as embryonic day (E) 14.5 and molecular analysis just before birth (E18.5) shows a lack of distal epithelium differentiation whereas proximal epithelium is unaffected. Electron microscopic analysis and glycogen staining confirm the lack of differentiation to mature Type II cells. Thus, elevated levels of GATA6 protein affect early lung development and in analogy to other GATA factors in other tissues, GATA6 also plays a crucial role in the terminal differentiation in this case of the distal pulmonary epithelium. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:105 / 114
页数:10
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