Evidence from normal expression and targeted misexpression that bone morphogenetic protein (Bmp-4) plays a role in mouse embryonic lung morphogenesis
| Autor: | S, Bellusci, R, Henderson, G, Winnier, T, Oikawa, B L, Hogan |
|---|---|
| Rok vydání: | 1996 |
| Předmět: |
Bone Morphogenetic Protein 7
Proteolipids Recombinant Fusion Proteins Molecular Sequence Data Gene Expression Mice Transgenic Wnt2 Protein Mesoderm Mice Transforming Growth Factor beta Proto-Oncogene Proteins Morphogenesis Animals Humans Hedgehog Proteins Lung DNA Primers Base Sequence Cell Death Nuclear Proteins Proteins Epithelial Cells Pulmonary Surfactants Rats DNA-Binding Proteins Mice Inbred C57BL Mice Inbred DBA Protein Biosynthesis Bone Morphogenetic Proteins Hepatocyte Nuclear Factor 3-beta Trans-Activators Cell Division Transcription Factors |
| Zdroj: | Development (Cambridge, England). 122(6) |
| ISSN: | 0950-1991 |
| Popis: | Epithelial-mesenchymal interactions are critical for the branching and differentiation of the lung, but the mechanisms involved are still unclear. To investigate this problem in mouse embryonic lung, we have studied the temporal and spatial expression of genes implicated in the morphogenesis of other organs. At 11.5 days p.c., hepatocyte nuclear factor-3beta (Hnf-3beta) is expressed uniformly throughout the epithelium, while Wnt-2 expression is confined to the distal mesenchyme. Sonic hedgehog (Shh) transcripts are found throughout the epithelium, with high levels in the distal tips of the terminal buds, while bone morphogenetic protein-4 (Bmp-4) transcripts are localized at high levels in the distal tips of the epithelium, with lower levels in the adjacent mesenchyme. Epithelial expression is also seen for Bmp-7, but transcripts are less dramatically upregulated at the distal tips. The Type I Bone morphogenetic protein receptor gene (Bmpr/Tfr-11/Brk-1) is expressed at low levels in the epithelium and in the distal mesenchyme. To investigate the role of Bmp-4 in lung development, we have misexpressed the gene throughout the distal epithelium of transgenic lungs using a surfactant protein C enhancer/promoter. From 15.5 days p.c., transgenic lungs are smaller than normal, with grossly distended terminal buds and, at birth, contain large air-filled sacs which do not support normal lung function. Labeling with BrdU reveals an inhibition of epithelia] proliferation in 15.5 days p.c. transgenic lungs. A small but significant stimulation of proliferation of mesenchymal cells is also observed, but this is accompanied by an increase in cell death. In situ hybridization with riboprobes for the proximal airway marker, CC10, and the distal airway marker, SP-C, shows normal differentiation of bronchiolar Clara cells but a reduction in the number of differentiated Type II cells in transgenic lungs. A model is proposed for the role of BMP4 and other signalling molecules in embryonic lung morphogenesis. |
| Databáze: | OpenAIRE |
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