The effects of dexamethasone on cigarette smoke induced gene expression changes in COPD macrophages

被引:18
作者
Kent, Lauren M. [1 ]
Fox, Steve M. [2 ]
Farrow, Stuart N. [2 ]
Singh, Dave [1 ]
机构
[1] Univ Manchester, Univ Hosp, NIHR Translat Res Facil, S Manchester Fdn Trust, Manchester M23 9LT, Lancs, England
[2] GlaxoSmithKline, Stevenage SG1 2NY, Herts, England
基金
英国生物技术与生命科学研究理事会;
关键词
COPD; Dexamethasone; Cytokine; Macrophage; Microarray; OBSTRUCTIVE PULMONARY-DISEASE; ALVEOLAR MACROPHAGES; CYTOKINE RELEASE; CHRONIC INHALATION; NUCLEAR RECEPTORS; OXIDATIVE STRESS; INHIBITION; LIPOPOLYSACCHARIDE; EXTRACT; ACTIVATION;
D O I
10.1016/j.intimp.2009.09.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Chronic obstructive pulmonary disease (COPD) is a smoking related inflammatory airway disease in which macrophages play a key role Previously we have shown that cigarette smoke extract (CSE) causes suppression of macrophage inflammatory mediators. with the exception of IL-8 We now investigate the effects of dexamethasone on these gene expression changes Monocyte derived macrophages (MDMs) were cultured with CSE and dexamethasone Microarray analysis was used to assess inflammatory mediator regulation, with qPCR and ELISA also performed for selected cytokines. The major effect of CSE was downregulation of inflammatory genes ( I I probe sets) For CSE regulated genes (n = 13), the median fold change with CSE alone was - 2 84 and with dexamethasone alone was - 2 97 Both treatments combined caused the greatest suppression of gene expression, - 4 47 qPCR also showed that IL-1 beta, GM-CSF and IL-6 mRNA levels were significantly reduced by CSE and further suppressed by dexamethasone qPCR and ELISA showed that IL-8 levels were increased by CSE. with suppression by dexamethasone We show that CSE suppressed the expression of some inflammatory genes whilst up-regulating IL-8 Dexamethasone further suppressed gene expression when combined with CSE The combined effect of GC and CSE causes Suppression of the macrophage innate immune response (C) 2009 Elsevier B V All rights reserved
引用
收藏
页码:57 / 64
页数:8
相关论文
共 51 条
[1]
Anzueto Antonio, 2007, Proc Am Thorac Soc, V4, P554, DOI 10.1513/pats.200701-003FM
[2]
Acute cigarette smoke exposure induces apoptosis of alveolar macrophages [J].
Aoshiba, K ;
Tamaoki, J ;
Nagai, A .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2001, 281 (06) :L1392-L1401
[3]
Corticosteroids: The drugs to beat [J].
Barnes, PJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 533 (1-3) :2-14
[4]
Corticosteroid resistance in chronic obstructive pulmonary disease: inactivation of histone deacetylase [J].
Barnes, PJ ;
Ito, K ;
Adcock, IM .
LANCET, 2004, 363 (9410) :731-733
[5]
New concepts in chronic obstructive pulmonary disease [J].
Barnes, PJ .
ANNUAL REVIEW OF MEDICINE, 2003, 54 :113-129
[6]
BIRREL M, 2003, J CELL PHYSL, V214, P27
[7]
The Maf transcription factors: regulators of differentiation [J].
Blank, V ;
Andrews, NC .
TRENDS IN BIOCHEMICAL SCIENCES, 1997, 22 (11) :437-441
[8]
Small Maf proteins in mammalian gene control: Mere dimerization partners or dynamic transcriptional regulators? [J].
Blank, Volker .
JOURNAL OF MOLECULAR BIOLOGY, 2008, 376 (04) :913-925
[9]
Salmeterol and fluticasone propionate and survival in chronic obstructive pulmonary disease [J].
Calverley, Peter M. A. ;
Anderson, Julie A. ;
Celli, Bartolome ;
Ferguson, Gary T. ;
Jenkins, Christine ;
Jones, Paul W. ;
Yates, Julie C. ;
Vestbo, Jorgen ;
Calverley, P. M. A. ;
Anderson, J. A. ;
Celli, B. ;
Ferguson, G. T. ;
Jenkins, C. ;
Jones, P. W. ;
Knobil, K. ;
Yates, J. C. ;
Vestbo, J. ;
Cherniack, R. ;
Similowski, T. ;
Cleland, J. ;
Whitehead, A. ;
Wise, R. ;
McGarvey, L. ;
John, M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (08) :775-789
[10]
Canine models of asthma and COPD [J].
Chapman, Richard W. .
PULMONARY PHARMACOLOGY & THERAPEUTICS, 2008, 21 (05) :731-742