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Published on: June 27, 2025
Pulmonary vascular disease is evident in gene regulation of experimental bronchopulmonary dysplasia
Cecilie Revhaug1,2, Magdalena Zasada3, Anne Gro W Rognlien1,2
1Department of Pediatric Research, University of Oslo, Oslo, Norway.
Insights
Bronchopulmonary dysplasia (BPD) in mice shows altered gene expression in pulmonary vasculature, indicating it
Area of Science:
- Pulmonary Medicine
- Genetics
- Neonatology
Background:
- Bronchopulmonary dysplasia (BPD) is a chronic lung disease in premature infants resulting from arrested alveolar development.
- While traditionally viewed as an airspace disease, the pulmonary vasculature's role in BPD pathology is increasingly recognized.
- Current understanding of BPD's disease process and effective treatments remains incomplete.
Purpose of the Study:
- To investigate gene expression patterns related to pulmonary vascular disease (PVD) in a mouse model of experimental BPD.
- To identify specific genes and pathways affected in the pulmonary vasculature during BPD development.
Main Methods:
- Utilized a murine model of hyperoxia-induced bronchopulmonary dysplasia.
- Employed gene expression microarray techniques to analyze mRNA expression in lung tissue.
- Combined gene expression pathway analysis and functional analysis of single gene transcripts to study PVD-related genes.
Main Results:
- Identified 117 significantly differentially regulated genes associated with PVD, involving contractile elements, vascular tone regulators, and tissue-specific genes.
- Observed down-regulation of the vasodilator gene Nppa (natriuretic peptide) and up-regulation of Pde1a, Ptger3, and Ptgs1.
- Pinpointed gene expression differences specifically within the pulmonary vasculature.
Conclusions:
- The pulmonary vasculature is significantly impacted by the arrested alveolar development characteristic of BPD.
- Differential gene expression in vascular tone and pulmonary vasculature suggests BPD involves more than just airspace abnormalities.
- Potential targets for BPD prevention and treatment may exist within the pulmonary vascular system.
Abstract:
Objective: To examine the gene expression regarding pulmonary vascular disease in experimental bronchopulmonary dysplasia in young mice. Premature delivery puts babies at risk of severe complications. Bronchopulmonary dysplasia (BPD) is a common complication of premature birth leading to lifelong affection of pulmonary function. BPD is recognized as a disease of arrested alveolar development. The disease process is not fully described and no complete cure or prevention is known. The focus of interest in the search for treatment and prevention of BPD has traditionally been at airspace level; however, the pulmonary vasculature is increasingly acknowledged in the pathology of BPD. The aim of the investigation was to study the gene expression in lungs with BPD with regards to pulmonary vascular disease (PVD).Methods: We employed a murine model of hyperoxia-induced BPD and gene expression microarray technique to determine the mRNA expression in lung tissue from young mice. We combined gene expression pathway analysis and analyzed the biological function of multiple single gene transcripts from lung homogenate to study the PVD relevant gene expression.Results: There were n = 117 significantly differentially regulated genes related to PVD through down-regulation of contractile elements, up- and down-regulation of factors involved in vascular tone and tissue-specific genes. Several genes also allowed for pinpointing gene expression differences to the pulmonary vasculature. The gene Nppa coding for a natriuretic peptide, a potent vasodilator, was significantly down-regulated and there was a significant up-regulation of Pde1a (phosphodiesterase 1A), Ptger3 (prostaglandin e receptor 3), and Ptgs1 (prostaglandin-endoperoxide synthase one).Conclusion: The pulmonary vasculature is affected by the arrest of secondary alveolarization as seen by differentially regulated genes involved in vascular tone and pulmonary vasculature suggesting BPD is not purely an airspace disease. Clues to prevention and treatment may lie in the pulmonary vascular system.
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