Linkage analysis of susceptibility to hyperoxia. Nrf2 is a candidate gene
- PMID: 11751202
- DOI: 10.1165/ajrcmb.26.1.4536
Linkage analysis of susceptibility to hyperoxia. Nrf2 is a candidate gene
Abstract
A strong role for reactive oxygen species (ROS) has been proposed in the pathogenesis of a number of lung diseases. Hyperoxia (> 95% oxygen) generates ROS and extensive lung damage, and has been used as a model of oxidant injury. However, the precise mechanisms of hyperoxia-induced toxicity have not been completely clarified. This study was designed to identify hyperoxia susceptibility genes in C57BL/6J (susceptible) and C3H/HeJ (resistant) mice. The quantitative phenotypes used for this analysis were pulmonary inflammatory cell influx, epithelial cell sloughing, and hyperpermeability. Genome-wide linkage analyses of intercross (F2) and recombinant inbred cohorts identified significant and suggestive quantitative trait loci on chromosomes 2 (hyperoxia susceptibility locus 1 [Hsl1]) and 3 (Hsl2), respectively. Comparative mapping of Hsl1 identified a strong candidate gene, Nfe2l2 (nuclear factor, erythroid derived 2, like 2 or Nrf2) that encodes a transcription factor NRF2 which regulates antioxidant and phase 2 gene expression. Strain-specific variation in lung Nrf2 messenger RNA expression and a T --> C substitution in the B6 Nrf2 promoter that cosegregated with susceptibility phenotypes in F2 animals supported Nrf2 as a candidate gene. Results from this study have important implications for understanding the mechanisms through which oxidants mediate the pathogenesis of lung disease.
Similar articles
-
Role of NRF2 in protection against hyperoxic lung injury in mice.Am J Respir Cell Mol Biol. 2002 Feb;26(2):175-82. doi: 10.1165/ajrcmb.26.2.4501. Am J Respir Cell Mol Biol. 2002. PMID: 11804867
-
Genetic susceptibility to ozone-induced lung hyperpermeability: role of toll-like receptor 4.Am J Respir Cell Mol Biol. 2000 May;22(5):620-7. doi: 10.1165/ajrcmb.22.5.3912. Am J Respir Cell Mol Biol. 2000. PMID: 10783135
-
Gene expression profiling of NRF2-mediated protection against oxidative injury.Free Radic Biol Med. 2005 Feb 1;38(3):325-43. doi: 10.1016/j.freeradbiomed.2004.10.013. Free Radic Biol Med. 2005. PMID: 15629862
-
Genetic mechanisms of susceptibility to oxidative lung injury in mice.Free Radic Biol Med. 2007 Feb 15;42(4):433-45. doi: 10.1016/j.freeradbiomed.2006.11.021. Epub 2006 Nov 23. Free Radic Biol Med. 2007. PMID: 17275675 Review.
-
Oxidative stress and antioxidants in the pathogenesis of pulmonary fibrosis: a potential role for Nrf2.Antioxid Redox Signal. 2008 Feb;10(2):321-32. doi: 10.1089/ars.2007.1901. Antioxid Redox Signal. 2008. PMID: 17999635 Review.
Cited by
-
Thioredoxin reductase inhibition elicits Nrf2-mediated responses in Clara cells: implications for oxidant-induced lung injury.Antioxid Redox Signal. 2012 Nov 15;17(10):1407-16. doi: 10.1089/ars.2011.4377. Epub 2012 Jun 25. Antioxid Redox Signal. 2012. PMID: 22607006 Free PMC article.
-
Genetic basis of murine responses to hyperoxia-induced lung injury.Immunogenetics. 2006 Oct;58(10):793-804. doi: 10.1007/s00251-006-0147-9. Epub 2006 Sep 26. Immunogenetics. 2006. PMID: 17001473 Free PMC article.
-
Mitochondrial DNA variation modulates alveolar development in newborn mice exposed to hyperoxia.Am J Physiol Lung Cell Mol Physiol. 2019 Dec 1;317(6):L740-L747. doi: 10.1152/ajplung.00220.2019. Epub 2019 Aug 21. Am J Physiol Lung Cell Mol Physiol. 2019. PMID: 31432715 Free PMC article.
-
The early responses of VEGF and its receptors during acute lung injury: implication of VEGF in alveolar epithelial cell survival.Crit Care. 2006;10(5):R130. doi: 10.1186/cc5042. Crit Care. 2006. PMID: 16968555 Free PMC article.
-
N-acetyl-lysyltyrosylcysteine amide, a novel systems pharmacology agent, reduces bronchopulmonary dysplasia in hyperoxic neonatal rat pups.Free Radic Biol Med. 2021 Apr;166:73-89. doi: 10.1016/j.freeradbiomed.2021.02.006. Epub 2021 Feb 17. Free Radic Biol Med. 2021. PMID: 33607217 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Miscellaneous