An FGF-WNT gene regulatory network controls lung mesenchyme development

被引:108
作者
Yin, Yongjun [1 ]
White, Andrew C. [1 ]
Huh, Sung-Ho [1 ]
Hilton, Matthew J. [2 ]
Kanazawa, Hidemi [1 ,2 ]
Long, Fanxin [1 ]
Ornitz, David M. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Dev Biol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Internal Med, St Louis, MO 63110 USA
关键词
fibroblast growth factor 9 (FGF9); fibroblast growth factor receptor (FGFR); WNT2a; WNT7b; beta-Catenin; lung development; mesenchyme;
D O I
10.1016/j.ydbio.2008.04.009
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lung mesenchyme is a critical determinant of the shape and size of the lung, the extent and patterning of epithelial branching, and the formation of the pulmonary vasculature and interstitial mesenchymal components of the adult lung. Fibroblast growth factor 9 (FGF9) is a critical regulator of lung mesenchymal growth; however, upstream mechanisms that modulate the FGF mesenchymal signal and the downstream targets of mesenchymal FGF signaling are poorly understood. Here we have identified a robust regulatory network in which mesenchymal FGF signaling regulates beta-Catenin mediated WNT signaling in lung mesenchyme. By conditionally inactivating beta-Catenin in lung mesenchyme, we show that mesenchymal WNT-beta-Catenin signaling is essential for lung development and acts to regulate the cell cycle G1 to S transition and the FGF responsiveness of mesenchyme. Together, both FGF and WNT signaling pathways function to sustain mesenchymal growth and coordinate epithelial morphogenesis during the pseudoglandular stage of lung development. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:426 / 436
页数:11
相关论文
共 56 条
[1]   CYCLIN D1 IS A NUCLEAR-PROTEIN REQUIRED FOR CELL-CYCLE PROGRESSION IN G(1) [J].
BALDIN, V ;
LUKAS, J ;
MARCOTE, MJ ;
PAGANO, M ;
DRAETTA, G .
GENES & DEVELOPMENT, 1993, 7 (05) :812-821
[2]  
Bellusci S, 1996, DEVELOPMENT, V122, P1693
[3]  
Bellusci S, 1997, DEVELOPMENT, V124, P4867
[4]   TCF: Lady justice casting the final verdict on the outcome of Wnt signalling [J].
Brantjes, H ;
Barker, N ;
van Es, J ;
Clevers, H .
BIOLOGICAL CHEMISTRY, 2002, 383 (02) :255-261
[5]  
Brault V, 2001, DEVELOPMENT, V128, P1253
[6]   The Wnt/β-catenin→Pitx2 pathway controls the turnover of Pitx2 and other unstable mRNAs [J].
Briata, P ;
Ilengo, C ;
Corte, G ;
Moroni, C ;
Rosenfeld, MG ;
Chen, CY ;
Gherzi, R .
MOLECULAR CELL, 2003, 12 (05) :1201-1211
[7]   Regulation of early lung morphogenesis:: questions, facts and controversies [J].
Cardoso, WV ;
Lü, JN .
DEVELOPMENT, 2006, 133 (09) :1611-1624
[8]  
Colvin JS, 1999, DEV DYNAM, V216, P72
[9]  
Colvin JS, 2001, DEVELOPMENT, V128, P2095
[10]   Dickkopf-1 (DKK1) reveals that fibronectin is a major target of Wnt signaling in branching morphogenesis of the mouse embryonic lung [J].
De Langhe, SP ;
Sala, FG ;
Del Moral, PM ;
Fairbanks, TJ ;
Yamada, KM ;
Warburton, D ;
Burns, RC ;
Bellusci, S .
DEVELOPMENTAL BIOLOGY, 2005, 277 (02) :316-331