β-Catenin promotes respiratory progenitor identity in mouse foregut

被引:154
作者
Harris-Johnson, Kelley S. [1 ]
Domyan, Eric T. [1 ]
Vezina, Chad M. [2 ]
Sun, Xin [1 ]
机构
[1] Univ Wisconsin, Genet Lab, Madison, WI 53706 USA
[2] Univ Wisconsin, Div Pharmaceut Sci, Madison, WI 53706 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
FGF; lung; progenitor cells; Wnt; RETINOIC ACID; BRANCHING MORPHOGENESIS; LUNG DEVELOPMENT; GENE; EXPRESSION; GROWTH; ROLES; LIVER; FGF; DIFFERENTIATION;
D O I
10.1073/pnas.0902274106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mammalian respiratory system, consisting of both trachea and lung, initiates from the foregut endoderm. The molecular program that instructs endodermal cells to adopt the respiratory fate is not fully understood. Here we show that conditional inactivation of beta-Catenin (also termed Ctnnb1) in foregut endoderm leads to absence of both the trachea and lung due to a failure in maintaining the respiratory fate. In converse, conditional expression of an activated form of beta-Catenin leads to expansion of Nkx2.1, an early marker for the trachea and lung, into adjacent endoderm including the stomach epithelium. Analyses of these mutants show that the loss or gain of trachea/ lung progenitor identity is accompanied by an expansion or contraction of esophagus/stomach progenitor identity, respectively. Our findings reveal an early role for beta-Catenin in the establishment of respiratory progenitors in mouse foregut endoderm.
引用
收藏
页码:16287 / 16292
页数:6
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