Nrf2 deficiency influences susceptibility to steroid resistance via HDAC2 reduction

被引:56
作者
Adenuga, David [1 ]
Caito, Samuel [1 ]
Yao, Hongwei [1 ]
Sundar, Isaac K. [1 ]
Hwang, Jae-Woong [1 ]
Chung, Sangwoon [1 ]
Rahman, Irfan [1 ]
机构
[1] Univ Rochester, Med Ctr, Dept Environm Med, Lung Biol & Dis Program, Rochester, NY 14642 USA
关键词
Cigarette smoke; Oxidant; Antioxidants; Nrf2; Inflammation; CIGARETTE-SMOKE; ANTIOXIDANT RESPONSE; HISTONE DEACETYLASE; LUNG INFLAMMATION; MICE; ACETYLATION; GENES; COPD; RECRUITMENT; ACTIVATION;
D O I
10.1016/j.bbrc.2010.11.054
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Abnormal lung inflammation and oxidant burden are associated with a significant reduction in histone deacetylase 2 (HDAC2) abundance and steroid resistance. We hypothesized that Nrf2 regulates steroid sensitivity via HDAC2 in response to inflammation in mouse lung. Furthermore, HDAC2 deficiency leads to steroid resistance in attenuating lung inflammatory response, which may be due to oxidant/antioxidant imbalance. Loss of antioxidant transcription factor Nrf2 resulted in decreased HDAC2 level in lung, and increased inflammatory lung response which was not reversed by steroid. Thus, steroid resistance or inability of steroids to control lung inflammatory response is dependent on Nrf2-HDAC2 axis. These findings have implications in steroid resistance, particularly during the conditions of oxidative stress when the lungs are more susceptible to inflammatory response, which is seen in patients with chronic obstructive pulmonary disease, asthma, rheumatoid arthritis, and inflammatory bowel disease. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:452 / 456
页数:5
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