Wnt/beta-catenin signaling acts upstream of N-myc, BMP4, and FGF signaling to regulate proximal-distal patterning in the lung.

Shu W, Guttentag S, Wang Z, Andl T, Ballard P, Lu MM, Piccolo S, Birchmeier W, Whitsett JA, Millar SE, Morrisey EE
Dev Biol. 2005 283 (1): 226-39

PMID: 15907834 · DOI:10.1016/j.ydbio.2005.04.014

Branching morphogenesis in the lung serves as a model for the complex patterning that is reiterated in multiple organs throughout development. Beta-catenin and Wnt signaling mediate critical functions in cell fate specification and differentiation, but specific functions during branching morphogenesis have remained unclear. Here, we show that Wnt/beta-catenin signaling regulates proximal-distal differentiation of airway epithelium. Inhibition of Wnt/beta-catenin signaling, either by expression of Dkk1 or by tissue-specific deletion of beta-catenin, results in disruption of distal airway development and expansion of proximal airways. Wnt/beta-catenin functions upstream of BMP4, FGF signaling, and N-myc. Moreover, we show that beta-catenin and LEF/TCF activate the promoters of BMP4 and N-myc. Thus, Wnt/beta-catenin signaling is a critical upstream regulator of proximal-distal patterning in the lung, in part, through regulation of N-myc, BMP4, and FGF signaling.

MeSH Terms (19)

Animals beta Catenin Body Patterning Bone Morphogenetic Protein 4 Bone Morphogenetic Proteins Cell Differentiation Cytoskeletal Proteins Fibroblast Growth Factors Gene Expression Regulation Intercellular Signaling Peptides and Proteins Lung Mice Mice, Inbred C57BL Morphogenesis Protein-Tyrosine Kinases Proto-Oncogene Proteins c-myc Signal Transduction Trans-Activators Wnt Proteins

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