Immune System Regulation Affected by a Murine Experimental Model of Bronchopulmonary Dysplasia: Genomic and Epigenetic Findings

Neonatology. 2019;116(3):269-277. doi: 10.1159/000501461. Epub 2019 Aug 27.

Abstract

Background: Bronchopulmonary dysplasia (BPD) is a common cause of abrupted lung development after preterm birth. BPD may lead to increased rehospitalization, more severe and frequent respiratory infections, and life-long reduced lung function. The gene regulation in lungs with BPD is complex, with various genetic and epigenetic factors involved.

Objectives: The aim of this study was to examine the regulatory relation between gene expression and the epigenome (DNA methylation) relevant for the immune system after hyperoxia followed by a recovery period in air using a mouse model of BPD.

Methods: Newborn mice pups were subjected to an immediate hyperoxic condition from birth and kept at 85% O2 levels for 14 days followed by a 14-day period in room air. Next, mice lung tissue was used for RNA and DNA extraction with subsequent microarray-based assessment of lung transcriptome and supplementary methylome analysis.

Results: The immune system-related transcriptomeregulation was affected in mouse lungs after hyperoxia. A high proportion of genes relevant in the immune system exhibited significant expression alterations, e.g., B cell-specific genes central to the cytokine-cytokine receptor interaction, the PI3K-AKT, and the B cell receptor signaling pathways. The findings were accompanied by significant DNA hypermethylation observed in the PI3K-AKT pathway and immune system-relevant genes.

Conclusions: Oxygen damage could be partly responsible for the increased susceptibility and abnormal response to respiratory viruses and infections seen in premature babies with BPD through dysregulated genes.

Keywords: Epigenetics; Experimental bronchopulmonary dysplasia; Gene regulation; Immune system regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptive Immunity / genetics
  • Animals
  • Animals, Newborn
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism
  • Bronchopulmonary Dysplasia / etiology
  • Bronchopulmonary Dysplasia / genetics*
  • Bronchopulmonary Dysplasia / immunology
  • Bronchopulmonary Dysplasia / metabolism
  • DNA Methylation*
  • Disease Models, Animal
  • Epigenesis, Genetic*
  • Hyperoxia / complications
  • Hyperoxia / genetics*
  • Hyperoxia / immunology
  • Hyperoxia / metabolism
  • Immunity, Innate / genetics
  • Lung / immunology*
  • Lung / metabolism
  • Mice, Inbred C57BL
  • Signal Transduction / genetics
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism
  • Transcriptome*