Conditional Gene Inactivation Reveals Roles for Fgf10 and Fgfr2 in Establishing a Normal Pattern of Epithelial Branching in the Mouse Lung

被引:122
作者
Abler, Lisa L. [1 ]
Mansour, Suzanne L. [2 ]
Sun, Xin [1 ]
机构
[1] Univ Wisconsin, Genet Lab, Madison, WI 53706 USA
[2] Univ Utah, Dept Human Genet, Salt Lake City, UT USA
关键词
Fgf10; Fgfr2; lung; development; branching morphogenesis; cell survival; proximal-distal patterning; FIBROBLAST-GROWTH-FACTOR; MORPHOGENETIC PROTEIN-4 BMP-4; SONIC HEDGEHOG; DEVELOPMENT SUGGESTS; CELL PROGENITORS; EXPRESSION; LIMB; DIFFERENTIATION; SOX2; MESENCHYME;
D O I
10.1002/dvdy.22032
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100123 [人体微生态学]; 100210 [外科学];
摘要
Fibroblast growth factor 10 (FGF10) signaling through FGF receptor 2 (FGFR2) is required for lung initiation. While studies indicate that Fgf10 and Fgfr2 are also important at later stages of lung development, their roles in early branching events remain unclear. We addressed this question through conditional inactivation of both genes in mouse subsequent to lung initiation. Inactivation of Fgf10 in lung mesenchyme resulted in smaller lobes with a reduced number of branches. Inactivation of Fgfr2 in lung epithelium resulted in disruption of lobes and small epithelial outgrowths that arose arbitrarily along the main bronchi. In both mutants, there was an increase in cell death. Also, the expression patterns of key signaling molecules implicated in branching morphogenesis were altered and a proximal lung marker was expanded distally. Our results indicate that both Fgt10 and Fgfr2 are required for a normal branching program and for proper proximal-distal patterning of the lung. Developmental Dynamics 238:1999-2013, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1999 / 2013
页数:15
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