OXIDATIVE INJURY OF CORONARY VENULAR ENDOTHELIAL-CELLS DEPLETES INTRACELLULAR GLUTATHIONE AND INDUCES HSP-70 MESSENGER-RNA

被引:24
作者
AUCOIN, MM
BARHOUMI, R
KOCHEVAR, DT
GRANGER, HJ
BURGHARDT, RC
机构
[1] TEXAS A&M UNIV, DEPT VET ANAT & PUBL HLTH, COLLEGE STN, TX 77843 USA
[2] TEXAS A&M UNIV, DEPT VET PHYSIOL & PHARMACOL, COLLEGE STN, TX 77843 USA
[3] TEXAS A&M UNIV, DEPT MED PHYSIOL, COLLEGE STN, TX 77843 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1995年 / 268卷 / 04期
关键词
MICROVASCULAR ENDOTHELIAL CELLS; OXIDATIVE STRESS; ANTIOXIDANT MECHANISMS; STRESS PROTEINS;
D O I
10.1152/ajpheart.1995.268.4.H1651
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vascular endothelium is one of the first tissues exposed to reactive oxygen species produced during myocardial ischemia-reperfusion. Bovine coronary venular endothelial cells (CVEC) were evaluated for intracellular glutathione (GSH) levels and heat shock protein 70 (HSP 70) mRNA and protein during in vitro oxidative stress. CVEC were incubated with 0.01875 U/ml xanthine oxidase (XO) and 0.5 mM hypoxanthine (HX) for 30 min and then allowed to recover for 0, 1, 2, or 3 h. Relative GSH levels were determined by evaluation of monochlorobimane fluorescence. GSH fluorescence was significantly lower in CVEC treated with XO + HX for 30 min than in controls. GSH fluorescence was also decreased in heat-shocked CVEC. After oxidative stress, GSH levels were higher than in controls at 1 h, but by 2 or 3 h after treatment, GSH fluorescence fell below control values. HSP 70 mRNA was induced in CVEC by a 30-min treatment with XO + HX followed by a 2- or 3-h recovery; however, HSP 70 protein was not significantly increased after XO + HX exposure. These data suggest that CVEC respond to oxidative stress by reducing intracellular GSH levels and inducing HSP 70 mRNA, although significant increases in HSP 70 protein were not detected at the time points tested.
引用
收藏
页码:H1651 / H1658
页数:8
相关论文
共 38 条
  • [11] ISCHEMIA OF THE DOG HEART INDUCES THE APPEARANCE OF A CARDIAC MESSENGER-RNA CODING FOR A PROTEIN WITH MIGRATION CHARACTERISTICS SIMILAR TO HEAT-SHOCK STRESS PROTEIN-71
    DILLMANN, WH
    MEHTA, HB
    BARRIEUX, A
    GUTH, BD
    NEELEY, WE
    ROSS, J
    [J]. CIRCULATION RESEARCH, 1986, 59 (01) : 110 - 114
  • [12] OXIDATIVE INJURY AND THE HEAT-SHOCK RESPONSE
    DONATI, YRA
    SLOSMAN, DO
    POLLA, BS
    [J]. BIOCHEMICAL PHARMACOLOGY, 1990, 40 (12) : 2571 - 2577
  • [13] SUPEROXIDE ANION RELEASE (O2-) AFTER ISCHEMIA AND REPERFUSION
    FREISCHLAG, JA
    HANNA, D
    [J]. JOURNAL OF SURGICAL RESEARCH, 1991, 50 (06) : 565 - 568
  • [14] GRISHAM MB, 1986, PHYSL OXYGEN RADICAL, P1
  • [15] ROLE OF GLUTATHIONE AND HSP-70 IN THE ACQUISITION OF THERMOTOLERANCE IN POSTIMPLANTATION RAT EMBRYOS
    HARRIS, C
    JUCHAU, MR
    MIRKES, PE
    [J]. TERATOLOGY, 1991, 43 (03) : 229 - 239
  • [16] EVALUATION OF METHODS FOR MEASURING CELLULAR GLUTATHIONE CONTENT USING FLOW-CYTOMETRY
    HEDLEY, DW
    CHOW, S
    [J]. CYTOMETRY, 1994, 15 (04): : 349 - 358
  • [17] LOCALIZATION OF XANTHINE-OXIDASE IN MAMMARY-GLAND EPITHELIUM AND CAPILLARY ENDOTHELIUM
    JARASCH, ED
    GRUND, C
    BRUDER, G
    HEID, HW
    KEENAN, TW
    FRANKE, WW
    [J]. CELL, 1981, 25 (01) : 67 - 82
  • [18] JARASCH ED, 1986, ACTA PHYSIOL SCAND, V126, P39
  • [19] HYPOXANTHINE XANTHINE OXIDASE-RELATED DEFECT IN POLYPEPTIDE-CHAIN INITIATION BY ENDOTHELIUM
    JORNOT, L
    JUNOD, AF
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1989, 66 (01) : 450 - 457
  • [20] DIFFERENTIAL EXPRESSION OF HSP70-STRESS PROTEINS IN HUMAN ENDOTHELIAL-CELLS EXPOSED TO HEAT-SHOCK AND HYDROGEN-PEROXIDE
    JORNOT, L
    MIRAULT, ME
    JUNOD, AF
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1991, 5 (03) : 265 - 275