Author/Authors :
Osoata، Grace O. نويسنده Airway Disease, National Heart and Lung Institute, Imperial College, London, UK, , , Ito، Misako نويسنده Airway Disease, National Heart and Lung Institute, Imperial College, London, UK , , Elliot، Mark S. نويسنده , , Hogg، James نويسنده The University of British Columbia, The James Hogg –iCAPTURE Center for Cardiovascular and Pulmonary Research, St. Pauls Hospital, Vancouver, Canada , , Barnes، Peter J. نويسنده Department of Thoracic Medicine, National Heart & Lung Institute, Imperial College, London, United Kingdom , , Ito، Kazuhiro نويسنده Airway Disease, National Heart and Lung Institute, Imperial College, London, UK ,
Abstract :
Background: Accumulation of nitrated protein is seen in peripheral lung and
cells from patients with chronic obstructive pulmonary disease (COPD).
Nitrated protein causes abnormal protein function, but the nitration was
believed to be an irreversible process. However, there are accumulating
evidences that this process is reversible by an active denitration pathway. The
aim of this study is to detect denitration activity in protein extracts from
peripheral lung tissue of COPD and to compare with those in healthy subjects.
Materials and Methods: Peripheral lung tissue from 4 healthy, 4 smokers
without COPD, 4 GOLD stage 1 and 4 GOLD stage 2 were used for denitration
assay. Denitration activity was determined as reduction of nitro-tyrosine level
of nitrated histone protein after incubation with protein extracts from
peripheral lung, which was determined by western blotting. In addition, RNA
is extracted from peripheral lung of 8 healthy, 7 smoking control, 8 stage 1 and
2 COPD and 10 stage 3 and 4 COPD and nitrate reductase mRNA expression
was determined by real time RT-PCR.
Results: Peripheral lung protein extracts from healthy subjects reduced nitrotyrosine
level of nitrated histone. Thus, we were able to show denitration
activity in peripheral lungs. The denitration activity was slightly reduced in
smoking controls, and significantly reduced in COPD patients. We also showed
that the expression of the human homologue of nitrate reductase (chytochrome
B2 reductase), a potential candidate of denitrase, was significanty reduced in
COPD lung.
Conclusion: This study suggests that accumulation of nitrated protein in lung
tissue of COPD may, at least in part, be induced by a reduction in denitration
activity or nitrate reductase.