Reduced nuclear factor-κB repressing factor: A link toward systemic inflammation in COPD

Kang Yun Lee, Shu Chuan Ho, Yao Fei Chan, Chun Hua Wang, Chien Da Huang, Wen Te Liu, Shu Min Lin, Yu Lun Lo, Ya Ling Chang, Lu Wei Kuo, Han Pin Kuo

研究成果: 雜誌貢獻文章

17 引文 (Scopus)

摘要

Chronic systemic inflammation is implicated in the systemic manifestations and, probably, the excess mortality risk of chronic obstructive pulmonary disease (COPD). The role of nuclear factor (NF)-κB repressing factor (NRF), a DNA-binding, protein-inhibiting NF-κB response gene, in human diseases has not been explored. We hypothesised that the NRF-negative regulatory mechanism is impaired in COPD peripheral blood mononuclear cells (PBMCs) leading to excessive interleukin (IL)-8/CXCL8 production. NRF expression, NF-κB activation, IL-8/CXCL8 release and intracellular oxidative stress were assessed in PBMCs of normal subjects and stable COPD patients. Primary PBMCs with NRF overexpression, NRF knockdown and exposure to H2O 2 were used to elucidate the mechanisms. Stable COPD patients, especially those with severe COPD, showed decreased NRF expression, enhanced NF-κB activation and increased IL-8/CXCL8 release in PBMCs compared with normal subjects. This was associated with reduced NRF and increased RNA polymerase II occupancy at the IL-8/CXCL8 promoter. NRF knockdown enhanced IL-8/CXCL8 production in normal PBMCs, whilst NRF overexpression attenuated IL-8/CXCL8 production. Intracellular oxidative stress was increased in COPD PBMCs. H2O2-decreased NRF expression and -enhanced IL-8/CXCL8 production was augmented in COPD PBMCs. NRF expression is reduced in PBMCs of stable COPD patients, probably through oxidative stress, leading to increased production of IL-8/CXCL8 and potentially chronic systemic inflammation. Copyright
原文英語
頁(從 - 到)863-873
頁數11
期刊European Respiratory Journal
40
發行號4
DOIs
出版狀態已發佈 - 十月 1 2012

指紋

Chronic Obstructive Pulmonary Disease
Interleukin-8
Inflammation
Blood Cells
Oxidative Stress
3'-(1-butylphosphoryl)adenosine
RNA Polymerase II
DNA-Binding Proteins
Mortality

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

引用此文

Reduced nuclear factor-κB repressing factor : A link toward systemic inflammation in COPD. / Lee, Kang Yun; Ho, Shu Chuan; Chan, Yao Fei; Wang, Chun Hua; Huang, Chien Da; Liu, Wen Te; Lin, Shu Min; Lo, Yu Lun; Chang, Ya Ling; Kuo, Lu Wei; Kuo, Han Pin.

於: European Respiratory Journal, 卷 40, 編號 4, 01.10.2012, p. 863-873.

研究成果: 雜誌貢獻文章

Lee, Kang Yun ; Ho, Shu Chuan ; Chan, Yao Fei ; Wang, Chun Hua ; Huang, Chien Da ; Liu, Wen Te ; Lin, Shu Min ; Lo, Yu Lun ; Chang, Ya Ling ; Kuo, Lu Wei ; Kuo, Han Pin. / Reduced nuclear factor-κB repressing factor : A link toward systemic inflammation in COPD. 於: European Respiratory Journal. 2012 ; 卷 40, 編號 4. 頁 863-873.
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abstract = "Chronic systemic inflammation is implicated in the systemic manifestations and, probably, the excess mortality risk of chronic obstructive pulmonary disease (COPD). The role of nuclear factor (NF)-κB repressing factor (NRF), a DNA-binding, protein-inhibiting NF-κB response gene, in human diseases has not been explored. We hypothesised that the NRF-negative regulatory mechanism is impaired in COPD peripheral blood mononuclear cells (PBMCs) leading to excessive interleukin (IL)-8/CXCL8 production. NRF expression, NF-κB activation, IL-8/CXCL8 release and intracellular oxidative stress were assessed in PBMCs of normal subjects and stable COPD patients. Primary PBMCs with NRF overexpression, NRF knockdown and exposure to H2O 2 were used to elucidate the mechanisms. Stable COPD patients, especially those with severe COPD, showed decreased NRF expression, enhanced NF-κB activation and increased IL-8/CXCL8 release in PBMCs compared with normal subjects. This was associated with reduced NRF and increased RNA polymerase II occupancy at the IL-8/CXCL8 promoter. NRF knockdown enhanced IL-8/CXCL8 production in normal PBMCs, whilst NRF overexpression attenuated IL-8/CXCL8 production. Intracellular oxidative stress was increased in COPD PBMCs. H2O2-decreased NRF expression and -enhanced IL-8/CXCL8 production was augmented in COPD PBMCs. NRF expression is reduced in PBMCs of stable COPD patients, probably through oxidative stress, leading to increased production of IL-8/CXCL8 and potentially chronic systemic inflammation. Copyright",
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T1 - Reduced nuclear factor-κB repressing factor

T2 - A link toward systemic inflammation in COPD

AU - Lee, Kang Yun

AU - Ho, Shu Chuan

AU - Chan, Yao Fei

AU - Wang, Chun Hua

AU - Huang, Chien Da

AU - Liu, Wen Te

AU - Lin, Shu Min

AU - Lo, Yu Lun

AU - Chang, Ya Ling

AU - Kuo, Lu Wei

AU - Kuo, Han Pin

PY - 2012/10/1

Y1 - 2012/10/1

N2 - Chronic systemic inflammation is implicated in the systemic manifestations and, probably, the excess mortality risk of chronic obstructive pulmonary disease (COPD). The role of nuclear factor (NF)-κB repressing factor (NRF), a DNA-binding, protein-inhibiting NF-κB response gene, in human diseases has not been explored. We hypothesised that the NRF-negative regulatory mechanism is impaired in COPD peripheral blood mononuclear cells (PBMCs) leading to excessive interleukin (IL)-8/CXCL8 production. NRF expression, NF-κB activation, IL-8/CXCL8 release and intracellular oxidative stress were assessed in PBMCs of normal subjects and stable COPD patients. Primary PBMCs with NRF overexpression, NRF knockdown and exposure to H2O 2 were used to elucidate the mechanisms. Stable COPD patients, especially those with severe COPD, showed decreased NRF expression, enhanced NF-κB activation and increased IL-8/CXCL8 release in PBMCs compared with normal subjects. This was associated with reduced NRF and increased RNA polymerase II occupancy at the IL-8/CXCL8 promoter. NRF knockdown enhanced IL-8/CXCL8 production in normal PBMCs, whilst NRF overexpression attenuated IL-8/CXCL8 production. Intracellular oxidative stress was increased in COPD PBMCs. H2O2-decreased NRF expression and -enhanced IL-8/CXCL8 production was augmented in COPD PBMCs. NRF expression is reduced in PBMCs of stable COPD patients, probably through oxidative stress, leading to increased production of IL-8/CXCL8 and potentially chronic systemic inflammation. Copyright

AB - Chronic systemic inflammation is implicated in the systemic manifestations and, probably, the excess mortality risk of chronic obstructive pulmonary disease (COPD). The role of nuclear factor (NF)-κB repressing factor (NRF), a DNA-binding, protein-inhibiting NF-κB response gene, in human diseases has not been explored. We hypothesised that the NRF-negative regulatory mechanism is impaired in COPD peripheral blood mononuclear cells (PBMCs) leading to excessive interleukin (IL)-8/CXCL8 production. NRF expression, NF-κB activation, IL-8/CXCL8 release and intracellular oxidative stress were assessed in PBMCs of normal subjects and stable COPD patients. Primary PBMCs with NRF overexpression, NRF knockdown and exposure to H2O 2 were used to elucidate the mechanisms. Stable COPD patients, especially those with severe COPD, showed decreased NRF expression, enhanced NF-κB activation and increased IL-8/CXCL8 release in PBMCs compared with normal subjects. This was associated with reduced NRF and increased RNA polymerase II occupancy at the IL-8/CXCL8 promoter. NRF knockdown enhanced IL-8/CXCL8 production in normal PBMCs, whilst NRF overexpression attenuated IL-8/CXCL8 production. Intracellular oxidative stress was increased in COPD PBMCs. H2O2-decreased NRF expression and -enhanced IL-8/CXCL8 production was augmented in COPD PBMCs. NRF expression is reduced in PBMCs of stable COPD patients, probably through oxidative stress, leading to increased production of IL-8/CXCL8 and potentially chronic systemic inflammation. Copyright

KW - Interleukin-8/CXCL8

KW - Oxidative stress

KW - Peripheral blood mononuclear cell

KW - RNA polymerase II

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