Peptidome analysis of lung tissues from a hyperoxia-induced bronchopulmonary dysplasia mouse model: Insights into the pathophysiological process of bronchopulmonary dysplasia

J Cell Physiol. 2018 Oct;233(10):7101-7112. doi: 10.1002/jcp.26633. Epub 2018 May 9.

Abstract

The aim of this study was to identify and compare the peptidomic profiles of lung tissues from neonatal mice with and without bronchopulmonary dysplasia (BPD). Hyperoxia was used to establish the BPD mouse model. Lung tissues obtained on postnatal day (PND) 9 were processed for analysis via histological staining and label-free liquid chromatography-mass spectrometry (LC-MS/MS). Histological analysis of the lung sections from the BPD group showed significant alveolar simplification and aberrant pulmonary vascularization. We identified 3,704 total peptides, of which 63 were differentially expressed in the lung tissues from the BPD group compared with those from the control group. Within this subset, 31 peptides were downregulated, and 32 peptides were upregulated. Bioinformatics analysis suggested several potential roles of the differentially expressed peptides in the pathophysiological process of BPD. In summary, this study highlights novel peptide candidates, and provides new insights for further understanding the molecular mechanism of BPD development.

Keywords: bronchopulmonary dysplasia (BPD); label-free liquid chromatography-mass spectrometry (LC-MS/MS); lung tissues; peptides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Bronchopulmonary Dysplasia / chemically induced
  • Bronchopulmonary Dysplasia / physiopathology*
  • Chromatography, Liquid / methods
  • Computational Biology / methods
  • Disease Models, Animal
  • Female
  • Humans
  • Hyperoxia / physiopathology*
  • Infant, Newborn
  • Lung / pathology
  • Lung / physiopathology*
  • Mice, Inbred C57BL
  • Tandem Mass Spectrometry / methods
  • Up-Regulation