In vivo exposure to hyperoxia induces DNA damage in a population of alveolar type II epithelial cells
- PMID: 14729512
- DOI: 10.1152/ajplung.00376.2003
In vivo exposure to hyperoxia induces DNA damage in a population of alveolar type II epithelial cells
Abstract
It is well established that hyperoxia injures and kills alveolar endothelial and type I epithelial cells of the lung. Although type II epithelial cells remain morphologically intact, it remains unclear whether they are also damaged. DNA integrity was investigated in adult mice whose type II cells were identified by their endogenous expression of pro-surfactant protein C or transgenic expression of enhanced green fluorescent protein. In mice exposed to room air, punctate perinuclear 8-oxoguanine staining was detected in approximately 4% of all alveolar cells and in 30% of type II cells. After 48 or 72 h of hyperoxia, 8-oxoguanine was detected in 11% of all alveolar cells and in >60% of type II cells. 8-Oxoguanine colocalized by confocal microscopy with the mitochondrial transmembrane protein cytochrome oxidase subunit 1. Type II cells isolated from hyperoxic lungs exhibited nuclear DNA strand breaks by comet assay even though they were viable and morphologically indistinguishable from cells isolated from lungs exposed to room air. These data reveal that type II cells exposed to in vivo hyperoxia have oxidized and fragmented DNA. Because type II cells are essential for lung remodeling, our findings raise the possibility that they are proficient in DNA repair.
Similar articles
-
Contribution of proliferation and DNA damage repair to alveolar epithelial type 2 cell recovery from hyperoxia.Am J Physiol Lung Cell Mol Physiol. 2006 Apr;290(4):L685-L694. doi: 10.1152/ajplung.00020.2005. Epub 2005 Nov 18. Am J Physiol Lung Cell Mol Physiol. 2006. PMID: 16299057
-
Neonatal hyperoxia stimulates the expansion of alveolar epithelial type II cells.Am J Respir Cell Mol Biol. 2014 Apr;50(4):757-66. doi: 10.1165/rcmb.2013-0207OC. Am J Respir Cell Mol Biol. 2014. PMID: 24188066 Free PMC article.
-
Type II epithelial cells are critical target for hyperoxia-mediated impairment of postnatal lung development.Am J Physiol Lung Cell Mol Physiol. 2006 Nov;291(5):L1101-11. doi: 10.1152/ajplung.00126.2006. Epub 2006 Jul 21. Am J Physiol Lung Cell Mol Physiol. 2006. PMID: 16861382
-
DNA damage and cell cycle checkpoints in hyperoxic lung injury: braking to facilitate repair.Am J Physiol Lung Cell Mol Physiol. 2001 Aug;281(2):L291-305. doi: 10.1152/ajplung.2001.281.2.L291. Am J Physiol Lung Cell Mol Physiol. 2001. PMID: 11435201 Review.
-
The use of alveolar epithelial type I cell-selective markers to investigate lung injury and repair.Eur Respir J. 2004 Oct;24(4):664-73. doi: 10.1183/09031936.04.00096003. Eur Respir J. 2004. PMID: 15459148 Review.
Cited by
-
Oxygen toxicity: cellular mechanisms in normobaric hyperoxia.Cell Biol Toxicol. 2023 Feb;39(1):111-143. doi: 10.1007/s10565-022-09773-7. Epub 2022 Sep 16. Cell Biol Toxicol. 2023. PMID: 36112262 Free PMC article. Review.
-
Contribution of neutrophils to acute lung injury.Mol Med. 2011 Mar-Apr;17(3-4):293-307. doi: 10.2119/molmed.2010.00138. Epub 2010 Oct 18. Mol Med. 2011. PMID: 21046059 Free PMC article. Review.
-
The RNA surveillance protein SMG1 activates p53 in response to DNA double-strand breaks but not exogenously oxidized mRNA.Cell Cycle. 2011 Aug 1;10(15):2561-7. doi: 10.4161/cc.10.15.16347. Epub 2011 Aug 1. Cell Cycle. 2011. PMID: 21701263 Free PMC article.
-
Epithelial ablation of Bcl-XL increases sensitivity to oxygen without disrupting lung development.Am J Respir Cell Mol Biol. 2010 Sep;43(3):376-85. doi: 10.1165/rcmb.2009-0165OC. Epub 2009 Oct 30. Am J Respir Cell Mol Biol. 2010. PMID: 19880821 Free PMC article.
-
PGC-1α activity and mitochondrial dysfunction in preterm infants.Front Physiol. 2022 Sep 26;13:997619. doi: 10.3389/fphys.2022.997619. eCollection 2022. Front Physiol. 2022. PMID: 36225305 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources