Oxidant stress suppresses CFTR expression

被引:86
作者
Cantin, AM
Bilodeau, G
Ouellet, C
Liao, J
Hanrahan, JW
机构
[1] Univ Sherbrooke, Fac Med, Pulm Res Unit, Sherbrooke, PQ J1H 5N4, Canada
[2] McGill Univ, Dept Physiol, Montreal, PQ, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2006年 / 290卷 / 01期
关键词
antioxidants; chloride channels; epithelial cells; cystic fibrosis; reactive oxygen species;
D O I
10.1152/ajpcell.00070.2005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epithelial mucous membranes are repeatedly exposed to oxidants and xenobiotics. CFTR plays a role in glutathione transepithelial flux and in defining the hydration and viscoelasticity of protective mucus. We therefore hypothesized that CFTR expression and function may be modulated by oxidant stress. A sublethal oxidant stress (tert-butylhydroquinone, BHQ) in CFTR-expressing epithelial cells (T84) induced a significant increase in cellular glutathione that was associated with an increase in expression of the gene encoding the heavy subunit of the rate-limiting enzyme for glutathione synthesis, gamma-glutamylcysteine synthetase (gamma-GCShs). CFTR gene expression was markedly decreased according to a time course that mirrored the changes in gamma-GCShs. Western blot analysis confirmed that the decrease in CFTR gene expression was associated with a decrease in CFTR protein. cAMP-dependent iodide efflux was also decreased by the oxidant stress. Nuclear run-on assays indicated that the oxidant stress had no effect on CFTR gene transcription, but the mRNA stability in the oxidant-stressed cells was markedly reduced. Furthermore, BHQ increased gamma-GCShs mRNA while decreasing CFTR mRNA in Calu-3 cells, and taurine chloramine induced similar effects in T84 cells. We conclude that suppression of CFTR expression may represent an adaptive response of mucosal epithelium to an exogenous oxidant stress.
引用
收藏
页码:C262 / C270
页数:9
相关论文
共 59 条
  • [41] PASSO SA, 1984, BLOOD, V63, P1361
  • [42] Reevaluating gel-forming mucins' roles in cystic fibrosis lung disease
    Perez-Vilar, J
    Boucher, RC
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2004, 37 (10) : 1564 - 1577
  • [43] Pilewski Joseph M., 1999, Physiological Reviews, V79, pS215
  • [44] Role of oxidants and antioxidants in the induction of AP-1, NF-kappa B, and glutathione S-transferase gene expression
    Pinkus, R
    Weiner, LM
    Daniel, V
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (23) : 13422 - 13429
  • [45] Puchelle Edith, 2002, Paediatr Respir Rev, V3, P115, DOI 10.1016/S1526-0550(02)00005-7
  • [46] Localization of γ-glutamylcysteine synthetase messenger RNA expression in lungs of smokers and patients with chronic obstructive pulmonary disease
    Rahman, I
    van Schadewijk, AAM
    Hiemstra, PS
    Stolk, J
    van Krieken, JHJM
    MacNee, W
    de Boer, WI
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (06) : 920 - 925
  • [47] Oxidative stress and regulation of glutathione in lung inflammation
    Rahman, I
    MacNee, W
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2000, 16 (03) : 534 - 554
  • [48] Lung glutathione and oxidative stress: implications in cigarette smoke-induced airway disease
    Rahman, I
    MacNee, W
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1999, 277 (06) : L1067 - L1088
  • [49] Induction of gamma-glutamylcysteine synthetase by cigarette smoke is associated with AP-1 in human alveolar epithelial cells
    Rahman, I
    Smith, CAD
    Lawson, MF
    Harrison, DJ
    MacNee, W
    [J]. FEBS LETTERS, 1996, 396 (01) : 21 - 25
  • [50] Retroviral transfer of MRP1 and γ-glutamyl cysteine synthetase modulates cell sensitivity to L-buthionine-S,R-sulphoximine (BSO):: new rationale for the use of BSO in cancer therapy
    Rappa, G
    Gamcsik, MP
    Mitina, RL
    Baum, C
    Fodstad, O
    Lorico, A
    [J]. EUROPEAN JOURNAL OF CANCER, 2003, 39 (01) : 120 - 128