Induction of heat shock protein 72 by a nitric oxide donor in guinea-pig gastric mucosal cells

被引:28
作者
Byrne, CR [1 ]
Hanson, PJ [1 ]
机构
[1] Aston Univ, Inst Pharmaceut Sci, Birmingham B4 7ET, W Midlands, England
基金
英国医学研究理事会;
关键词
nitric oxide (NO); gastric mucose; stomach; heat shock protein;
D O I
10.1016/S0014-2999(98)00388-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gastric mucosal cells may be exposed to exogenous nitric oxide (NO) from a variety of sources. The response of primary cultures of guinea-pig gastric mucosal cells to the NO donor S-nitroso-N-acetyl-penicillamine was therefore investigated. Exposure to S-nitroso-N-acetyl-penicillamine for 8 h caused a concentration-dependent induction of heat shock protein 72 (HSP 72). Induction was inhibited by the NO scavenger 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, and by blockade of transcription with actinomycin D. Induction of HSP 72 by S-nitroso-N-acetyl-penicillamine was enhanced by diethyl maleate which decreased the intracellular reduced thiol content. By contrast, HSP 72 formation after heat shock was associated with an elevation of reduced thiol. Incubation with S-nitroso-N-acetyl-penicillamine for 18 h increased detachment of cells from the culture plate. The effect of S-nitroso-N-acetyl-penicillamine on detachment was exacerbated by the presence of actinomycin D. In conclusion, exogenous NO induces HSP 72 in guinea-pig gastric mucosal cells and this response may in part protect the cells from the deleterious effects of NO. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:117 / 122
页数:6
相关论文
共 19 条
[1]   NITRIC-OXIDE GENERATORS AND CGMP STIMULATE MUCUS SECRETION BY RAT GASTRIC-MUCOSAL CELLS [J].
BROWN, JF ;
KEATES, AC ;
HANSON, PJ ;
WHITTLE, BJR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (03) :G418-G422
[2]   LIPOPOLYSACCHARIDE INDUCES CA2+-INDEPENDENT NITRIC-OXIDE SYNTHASE ACTIVITY IN RAT GASTRIC-MUCOSAL CELLS [J].
BROWN, JF ;
TEPPERMAN, BL ;
HANSON, PJ ;
WHITTLE, BJR .
EUROPEAN JOURNAL OF PHARMACOLOGY-ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY SECTION, 1994, 292 (01) :111-114
[3]   Heat shock proteins and macrophage resistance to the toxic effects of nitric oxide [J].
Hirvonen, MR ;
Brune, B ;
Lapetina, EG .
BIOCHEMICAL JOURNAL, 1996, 315 :845-849
[4]  
HUANG LE, 1994, J BIOL CHEM, V269, P30718
[5]  
HUBER W, 1993, AM J PHYSIOL, V265, pG1021, DOI 10.1152/ajpgi.1993.265.6.G1021
[6]   Nitric oxide protects cultured rat hepatocytes from tumor necrosis factor-alpha-induced apoptosis by inducing heat shock protein 70 expression [J].
Kim, YM ;
deVera, ME ;
Watkins, SC ;
Billiar, TR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (02) :1402-1411
[7]   MULTIPLE FUNCTIONS OF NITRIC-OXIDE IN PATHOPHYSIOLOGY AND MICROBIOLOGY - ANALYSIS BY A NEW NITRIC-OXIDE SCAVENGER [J].
MAEDA, H ;
AKAIKE, T ;
YOSHIDA, M ;
SUGA, M .
JOURNAL OF LEUKOCYTE BIOLOGY, 1994, 56 (05) :588-592
[8]   Nitric oxide donor induces HSP70 accumulation in the heart and in cultured cells [J].
Malysheva, IY ;
Malugin, AV ;
Golubeva, LY ;
Zenina, TA ;
Manukhina, EB ;
Mikoyan, VD ;
Vanin, AF .
FEBS LETTERS, 1996, 391 (1-2) :21-23
[9]  
Mannick EE, 1996, CANCER RES, V56, P3238
[10]   Chemical synthesis of nitric oxide in the stomach from dietary nitrate in humans [J].
McKnight, GM ;
Smith, LM ;
Drummond, RS ;
Duncan, CW ;
Golden, M ;
Benjamin, N .
GUT, 1997, 40 (02) :211-214