Your browser doesn't support javascript.
loading
Pulmonary vascular disease is evident in gene regulation of experimental bronchopulmonary dysplasia.
Revhaug, Cecilie; Zasada, Magdalena; Rognlien, Anne Gro W; Günther, Clara-Cecilie; Grabowska, Agnieszka; Ksiazek, Teofila; Madetko-Talowska, Anna; Szewczyk, Katarzyna; Bik-Multanowski, Mirolaw; Kwinta, Przemko; Pietrzyk, Jacek J; Baumbusch, Lars O; Saugstad, Ola D.
Afiliação
  • Revhaug C; Department of Pediatric Research, University of Oslo, Oslo, Norway.
  • Zasada M; Department of Pediatric Research, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
  • Rognlien AGW; Department of Pediatrics, Institute of Pediatrics, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.
  • Günther CC; Department of Pediatric Research, University of Oslo, Oslo, Norway.
  • Grabowska A; Department of Pediatric Research, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
  • Ksiazek T; Norwegian Computing Center, Oslo, Norway.
  • Madetko-Talowska A; Department of Medical Genetics, Institute of Pediatrics, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.
  • Szewczyk K; Department of Medical Genetics, Institute of Pediatrics, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.
  • Bik-Multanowski M; Department of Medical Genetics, Institute of Pediatrics, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.
  • Kwinta P; Department of Medical Genetics, Institute of Pediatrics, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.
  • Pietrzyk JJ; Department of Medical Genetics, Institute of Pediatrics, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.
  • Baumbusch LO; Department of Pediatrics, Institute of Pediatrics, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.
  • Saugstad OD; Department of Pediatrics, Institute of Pediatrics, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.
J Matern Fetal Neonatal Med ; 33(12): 2122-2130, 2020 Jun.
Article em En | MEDLINE | ID: mdl-30428746
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.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / Displasia Broncopulmonar / RNA Mensageiro / Pulmão Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: J Matern Fetal Neonatal Med Assunto da revista: OBSTETRICIA / PERINATOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Noruega País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / Displasia Broncopulmonar / RNA Mensageiro / Pulmão Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: J Matern Fetal Neonatal Med Assunto da revista: OBSTETRICIA / PERINATOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Noruega País de publicação: Reino Unido