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Reduced Denitration Activity in Peripheral Lung of Chronic Obstructive Pulmonary Disease

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 evidence...

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Autores principales: Osoata, Grace O., Ito, Misako, Elliot, Mark, Hogg, James, Barnes, Peter J., Ito, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Research Institute of Tuberculosis and Lung Disease 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153218/
https://www.ncbi.nlm.nih.gov/pubmed/25191434
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author Osoata, Grace O.
Ito, Misako
Elliot, Mark
Hogg, James
Barnes, Peter J.
Ito, Kazuhiro
author_facet Osoata, Grace O.
Ito, Misako
Elliot, Mark
Hogg, James
Barnes, Peter J.
Ito, Kazuhiro
author_sort Osoata, Grace O.
collection PubMed
description 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 nitro-tyrosine 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 β2 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.
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spelling pubmed-41532182014-09-04 Reduced Denitration Activity in Peripheral Lung of Chronic Obstructive Pulmonary Disease Osoata, Grace O. Ito, Misako Elliot, Mark Hogg, James Barnes, Peter J. Ito, Kazuhiro Tanaffos Original Article 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 nitro-tyrosine 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 β2 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. National Research Institute of Tuberculosis and Lung Disease 2012 /pmc/articles/PMC4153218/ /pubmed/25191434 Text en Copyright © 2012 National Research Institute of Tuberculosis and Lung Disease http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Osoata, Grace O.
Ito, Misako
Elliot, Mark
Hogg, James
Barnes, Peter J.
Ito, Kazuhiro
Reduced Denitration Activity in Peripheral Lung of Chronic Obstructive Pulmonary Disease
title Reduced Denitration Activity in Peripheral Lung of Chronic Obstructive Pulmonary Disease
title_full Reduced Denitration Activity in Peripheral Lung of Chronic Obstructive Pulmonary Disease
title_fullStr Reduced Denitration Activity in Peripheral Lung of Chronic Obstructive Pulmonary Disease
title_full_unstemmed Reduced Denitration Activity in Peripheral Lung of Chronic Obstructive Pulmonary Disease
title_short Reduced Denitration Activity in Peripheral Lung of Chronic Obstructive Pulmonary Disease
title_sort reduced denitration activity in peripheral lung of chronic obstructive pulmonary disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153218/
https://www.ncbi.nlm.nih.gov/pubmed/25191434
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