Hyperoxia-Exposed Lung Injury Upregulates DVL-1 Protein Expression And Activates Wnt/β-Catenin Signaling Pathway in Newborn Rat Lung

Abstract Background: Bronchopulmonary dysplasia (BPD) is a serious and lifelong pulmonary disease in premature neonates, which has an influence on a quarter of premature newborns. Wingless/integrated(Wnt)/β-catenin signaling pathway affects lung cell differentiation and lung tissue structure, and is abnormal activation in the lungs of rats with pulmonary fibrosis. Method: Newborn rats were subjected to hyperoxia-exposure, histopathological changes in lung tissues were evaluated through Immunohistochemistry (IHC), Dishevelled (DVL-1) and signaling pathways were detected through western blotting and real-time PCR. Results: Contrasting with the normoxic lungs, hyperoxia-exposed lungs demonstrated larger alveoli, less alveoli and thicker alveolar septa, and the number of alveoli reduced obviously, alveoli enlarged seriously in hyperoxia group. SOD activity was decreased (7 th day: P < 0.05; 14 th day: P < 0.01), and MDA was increased (7 th day: P < 0.05; 14 th day: P < 0.01) after hyperoxia exposure. Protein and mRNA expression levels of β-catenin, DVL-1, Ctnnbl1 and Cyclin D1 were upregulated by hyperoxia exposure on 7 th day( P < 0.01) and 14 th day( P < 0.01). Conclusion: We confirmed the positive role of DVL-1 and Wnt/β-catenin signaling pathway in promoting BPD under hyperoxia conditions, and provided promising therapeutic targets in the future.