Exposure to Hyperoxia Induces p53 Expression in Mouse Lung Epithelium
- 1 January 1998
- journal article
- Published by American Thoracic Society in American Journal of Respiratory Cell and Molecular Biology
- Vol. 18 (1) , 43-50
- https://doi.org/10.1165/ajrcmb.18.1.2950m
Abstract
Cells that are exposed to free radicals have increased levels of DNA strand breaks with accumulation of the tumor suppressor protein p53, which induces cell cycle arrest and/or apoptosis. Because oxidants injure pulmonary epithelial cells, it was hypothesized that exposure to hyperoxia promotes DNA strand breaks in lung epithelium, resulting in increased expression of p53 and loss of epithelial cell function. Adult male C57Bl/6J mice were exposed to . 95% oxygen for 72 h and DNA integrity was determined in their lungs by terminal transferase immunoreactivity. Both nonimmunoreactive and lightly stained nuclei were ob- served in cells comprising the airway and parenchyma. Exposure to hyperoxia resulted in a marked in- crease in the intensity of nuclear staining in distal bronchiolar epithelium and alveolar epithelial and endo- thelial cells. Airway epithelial cells from control lungs contained detectable levels of p53 protein, which markedly increased in both nuclei and cytoplasm of distal bronchiolar epithelial cells and to a lesser extent in alveolar epithelial cells that were morphologically consistent with type II cells. Western and Northern blot analyses revealed that hyperoxia increased total lung p53 protein expression but not levels of mRNA. Changes in terminal transferase immunoreactivity and p53 expression were not observed in large airway cells, fibroblasts underlying distal airway, or smooth muscle cells. Expression of SP-B mRNA modestly increased and Clara cell secretory protein and cytochrome P -450 2F2 mRNAs decreased, providing addi- tional evidence that hyperoxia injured pulmonary epithelial cells. These findings support the concept that hyperoxia damages DNA of pulmonary epithelial cells, which respond by accumulating p53 and changes in epithelial cell-specific gene expression. O'Reilly, M. A., R. J. Staversky, B. R. Stripp, and J. N. Finkelstein. 1998. Exposure to hyperoxia induces p53 expression in mouse lung epithelium. Am. J. Respir. Cell Mol. Biol. 18:43-50.Keywords
This publication has 21 references indexed in Scilit:
- Cell Cycle Checkpoints: Preventing an Identity CrisisScience, 1996
- Cellular Oxygen ToxicityJournal of Biological Chemistry, 1996
- Importance of SE-glutathione peroxidase, catalase, and CU/ZN-SOD for cell survival against oxidative stressFree Radical Biology & Medicine, 1994
- Antigen retrieval technique utilizing citrate buffer or urea solution for immunohistochemical demonstration of androgen receptor in formalin-fixed paraffin sections.Journal of Histochemistry & Cytochemistry, 1993
- Inter-strain variation in susceptibility to hyperoxic injury of murine airwaysPharmacogenetics, 1993
- In situ end‐labelling detects DNA strand breaks in apoptosis and other physiological and pathological statesThe Journal of Pathology, 1993
- The p53 tumour suppressor geneNature, 1991
- Genetic toxicology of oxygenMutation Research/DNAging, 1989
- DNA Damage and Oxygen Radical ToxicityScience, 1988
- Morphologic Changes in Pulmonary Oxygen ToxicityAnnual Review of Physiology, 1986