Journal
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY
Volume 322, Issue 1, Pages L33-L49Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajplung.00237.2021
Keywords
airway macrophages; gene-environment interactions; mouse; ozone; transcriptomics
Categories
Funding
- NIH [ES024965, ES024965-S1]
- UNC Center for Environmental Health and Susceptibility Pilot Project Award [P30ES010126]
- T32 training grants [ES00712635]
- Leon and Bertha Golberg Postdoctoral Fellowship from the UNC Curriculum in Toxicology and Environmental Medicine
- UNC Dissertation Completion Fellowships
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This study aimed to explore the effects of strain, exposure, and strain-by-O3 exposure interactions on airway macrophage (AM) gene expression, as well as to identify transcriptional correlates of O3-induced inflammation and injury. The results showed that O3 exposure resulted in airway neutrophilia and lung injury, with differences in gene expression between different strains likely contributing to their varying responses to O3.
Acute ozone (O3) exposure is associated with multiple adverse cardiorespiratory outcomes, the severity of which varies across individuals in human populations and inbred mouse strains. However, molecular determinants of response, including susceptibility biomarkers that distinguish who will develop severe injury and inflammation, are not well characterized. We and others have demonstrated that airway macrophages (AMs) are an important resident immune cell type that are functionally and transcriptionally responsive to O3 inhalation. Here, we sought to explore influences of strain, exposure, and strain-by-O3 exposure interactions on AM gene expression and identify transcriptional correlates of O3-induced inflammation and injury across six mouse strains, including five Collaborative Cross (CC) strains. We exposed adult mice of both sexes to filtered air (FA) or 2 ppm O3 for 3 h and measured inflammatory and injury parameters 21 h later. Mice exposed to O3 developed airway neutrophilia and lung injury with strain-dependent severity. In AMs, we identified a common core O3 transcriptional response signature across all strains, as well as a set of genes exhibiting strain-by-O3 exposure interactions. In particular, a prominent gene expression contrast emerged between a low- (CC017/Unc) and high-responding (CC003/Unc) strain, as reflected by cellular inflammation and injury. Further inspection indicated that differences in their baseline gene expression and chromatin accessibility profiles likely contribute to their divergent post-O3 exposure transcriptional responses. Together, these results suggest that aspects of O3induced respiratory responses are mediated through altered AM transcriptional signatures and further confirm the importance of gene-environment interactions in mediating differential responsiveness to environmental agents.
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