Genome‐wide association mapping of acute lung injury in neonatal inbred mice. Issue 6 (26th February 2014)

• Record Type: Journal Article
• Authors: Nichols, Jennifer L.; Gladwell, Wesley; Verhein, Kirsten C.; Cho, Hye‐Youn; Wess, Jürgen; Suzuki, Oscar; Wiltshire, Tim; Kleeberger, Steven R.
• Is Part Of: FASEB journal. Volume 28:Issue 6(2014)
• Page Start: 2538
• Page End: 2550
• Publication Date: 2014-02-26
• Subjects: bronchopulmonary dysplasia -- inflammation -- quantitative trait locus -- cholinergic receptor -- muscarinic 2 -- cardiac; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.13-247221
• Languages: English
• ISSNs: 0892-6638

Abstract

ABSTRACT: Reactive oxygen species (ROS) contribute to the pathogenesis of many acute and chronic pulmonary disorders, including bronchopulmonary dysplasia (BPD), a respiratory condition that affects preterm infants. However, the mechanisms of susceptibility to oxidant stress in neonatal lungs are not completely understood. We evaluated the role of genetic background in response to oxidant stress in the neonatal lung by exposing mice from 36 inbred strains to hyperoxia (95% O2 ) for 72 h after birth. Hyperoxia‐induced lung injury was evaluated by using bronchoalveolar lavage fluid (BALF) analysis and pathology. Statistically significant interstrain variation was found for BALF inflammatory cells and protein (heritability estimates range: 33.6–55.7%). Genome‐wide association mapping using injury phenotypes identified quantitative trait loci (QTLs) on chromosomes 1, 2, 4, 6, and 7. Comparative mapping of the chromosome 6 QTLs identified Chrm2 (cholinergic receptor, muscarinic 2, cardiac) as a candidate susceptibility gene, and mouse strains with a nonsynonymous coding single‐nucleotide polymorphism (SNP) in Chrm2 that causes an amino acid substitution (P265L) had significantly reduced hyperoxia‐induced inflammation compared to strains without the SNP. Further, hyperoxia‐induced lung injury was significantly reduced in neonatal mice with targeted deletion of Chrm2, relative to wild‐type controls. This study has important implications for understanding the mechanisms of oxidative lung injury in neonates.—Nichols, J. L., Gladwell, W., Verhein, K. C., Cho, H.‐Y., Wess, J., Suzuki, O., Wiltshire, T., Kleeberger, S. R. Genome‐wide association mapping of acute lung injury in neonatal inbred mice. FASEB J . 28, 2538–2550 (2014). www.fasebj.org