Transcriptional Profiling of the Murine Airway Response to Acute Ozone Exposure. (18th October 2019)

• Record Type: Journal Article
• Authors: Tovar, Adelaide; Smith, Gregory J; Thomas, Joseph M; Crouse, Wesley L; Harkema, Jack R; Kelada, Samir N P
• Is Part Of: Toxicological sciences. Volume 173:Number 1(2020)
• Page Start: 114
• Page End: 130
• Publication Date: 2019-10-18
• Subjects: ozone -- air pollution -- transcriptomics -- lung -- inflammation -- injury -- mouse; Toxicology -- Periodicals; Toxicology -- Periodicals; Toxicology; Periodicals; 615.9
• DOI: 10.1093/toxsci/kfz219
• Languages: English
• ISSNs: 1096-6080

Abstract

Abstract: Ambient ozone (O3 ) exposure has serious consequences on respiratory health, including airway inflammation and injury. Decades of research have yielded thorough descriptions of these outcomes; however, less is known about the molecular processes that drive them. The aim of this study was to further describe the cellular and molecular responses to O3 exposure in murine airways, with a particular focus on transcriptional responses in 2 critical pulmonary tissue compartments: conducting airways (CA) and airway macrophages (AM). After exposing adult, female C57BL/6J mice to filtered air, 1 or 2 ppm O3, we assessed hallmark responses including airway inflammation (cell counts and cytokine secretion) and injury (epithelial permeability), followed by gene expression profiling of CA and AM by RNA-seq. As expected, we observed concentration-dependent increases in airway inflammation and injury. Conducting airways and AM both exhibited changes in gene expression to both 1 and 2 ppm O3 that were largely compartment-specific. In CA, genes associated with epithelial barrier function, detoxification processes, and cellular proliferation were altered, while O3 affected genes involved in innate immune signaling, cytokine production, and extracellular matrix remodeling in AM. Further, CA and AM also exhibited notable differences in concentration–response expression patterns for large numbers of genes. Overall, our study has described transcriptional responses to acute O3 exposure, revealing both shared and unique gene expression patterns across multiple concentrations of O3 and in 2 important O3 -responsive tissues. These profiles provide broad mechanistic insight into pulmonary O3 toxicity, and reveal a variety of targets for focused follow-up studies.