Oxidative Damage to Nucleic Acids in Severe Emphysema
Background: Oxidative stress is a key element in the pathogenesis of emphysema, but oxidation of nucleic acids has been largely overlooked. The aim of this study was to investigate oxidative damage to nucleic acids in severe emphysematous lungs. Methods: Thirteen human severe emphysematous lungs, in...
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Veröffentlicht in: | Chest 2009-04, Vol.135 (4), p.965-974 |
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Zusammenfassung: | Background: Oxidative stress is a key element in the pathogenesis of emphysema, but oxidation of nucleic acids has been largely overlooked.
The aim of this study was to investigate oxidative damage to nucleic acids in severe emphysematous lungs.
Methods: Thirteen human severe emphysematous lungs, including five with α 1 -antitrypsin deficiency (AATD), were obtained from patients receiving lung transplantation. Control lung tissue was obtained
from non-COPD lungs (n = 8) and donor lungs (n = 8). DNA and RNA oxidation were investigated by immunochemistry. Morphometry
(mean linear intercept [Lm] and CT scan) and immunostaining for CD68 and neutrophil elastase also were performed.
Results: Nucleic acid oxidation was increased in alveolar wall cells in emphysematous lungs compared to non-COPD and donor lungs (p
< 0.01). In emphysematous lungs, oxidative damage to nucleic acids in alveolar wall cells was increased in the more severe
emphysematous areas assessed by histology (Lm, > 0.5 mm; p < 0.05) and CT scan (< â950 Hounsfield units; p < 0.05). Compared
to classic emphysema, AATD lungs exhibited higher levels of nucleic acid oxidation in macrophages (p < 0.05) and airway epithelial
cells (p < 0.01). Pretreatments with DNase and RNase demonstrated that RNA oxidation was more prevalent than DNA oxidation
in alveolar wall cells.
Conclusions: We demonstrated for the first time that nucleic acids, especially RNA, are oxidized in human emphysematous lungs. The correlation
between the levels of oxidative damage to nucleic acids in alveolar wall cells and the severity of emphysema suggest a potential
role in the pathogenesis of emphysema. |
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ISSN: | 0012-3692 1931-3543 |
DOI: | 10.1378/chest.08-2257 |