Zinc-related metallothionein metabolism in bovine pulmonary artery endothelial cells

被引:17
作者
Bobilya, DJ
Reynolds, JT
Faia, KL
Briske-Anderson, M
Reeves, PG
机构
[1] Univ New Hampshire, Dept Anim & Nutr Sci, Durham, NH 03824 USA
[2] USDA ARS, Grand Forks Human Nutr Res Ctr, Grand Forks, ND 58202 USA
基金
美国国家卫生研究院;
关键词
metallothionein; zinc; endothelial cell; IL-6; dexamethasone; 17; beta-estradiol;
D O I
10.1016/S0955-2863(98)00099-0
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
Bovine pulmonary artery endothelial cells (BPAEC) were cultured in vitro under a variety of conditions to investigate holy metallothionein (MT) might participate in zinc homeostasis. Experimental conditions included 10% serum to ensure that the in vitro environment would be a better reflection of the in vivo situation than with protein-free medium. MT was increased by acutely high zinc concentrations (100-200 mu mol/L) in the extracellular environment, MT was relatively insensitive to moderate changes in zinc concentration (2-50 mu mol/L), even after prolonged exposure for 7 to 12 days. BPAEC had reduced MT content when grown in medium containing serum that had been dialyzed to remove components with a molecular mass of less than 1,000, including zinc. Because the principal source of the major minerals in the experimental medium was nor the serum, their concentrations in the final medium were not significantly influenced by serum dialysis. Restoring the zinc concentration in the medium containing the dialyzed serum did not restore MT content in BPAEC, suggesting that some small molecular weight molecule other than zinc established their basal MT content. This study did not identify these putative factors in serum, but hormones are likely candidates. Forty-eight-hour incubations of BPAEC with interleukin (IL-6) or dexamethasone increased cellular MT; however, 17 beta-estradiol decreased MT, and IL-l and adenosine 3',5'-cyclic phosphate (cAMP) had ilo discernible effect. We conclude that extracellular zinc concentrations have relatively little impact on the cellular concentrations of MT and zinc of BPAEC in vitro. Zinc homeostasis by BPAEC is not maintained by changing the MT concentration in response to changes in the extracellular zinc environment. (C) Elsevier Science Inc. 1999. All rights reserved.
引用
收藏
页码:139 / 145
页数:7
相关论文
共 25 条
  • [1] LEVELS OF METALLOTHIONEIN MESSENGER-RNA IN FETAL, NEONATAL AND MATERNAL RAT-LIVER
    ANDERSEN, RD
    PILETZ, JE
    BIRREN, BW
    HERSCHMAN, HR
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1983, 131 (03): : 497 - 500
  • [2] METALLOTHIONEIN GENE-EXPRESSION IN RATS - TISSUE-SPECIFIC REGULATION BY DIETARY COPPER AND ZINC
    BLALOCK, TL
    DUNN, MA
    COUSINS, RJ
    [J]. JOURNAL OF NUTRITION, 1988, 118 (02) : 222 - 228
  • [3] ZINC TRANSPORT INTO ENDOTHELIAL-CELLS IS A FACILITATED PROCESS
    BOBILYA, DJ
    BRISKEANDERSON, M
    REEVES, PG
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 1992, 151 (01) : 1 - 7
  • [4] BREMNER I, 1991, METHOD ENZYMOL, V205, P25
  • [5] Cousins R.J., 1996, PRESENT KNOWLEDGE NU, V7th, P293
  • [6] COORDINATE REGULATION OF ZINC-METABOLISM AND METALLOTHIONEIN GENE-EXPRESSION IN RATS
    COUSINS, RJ
    DUNN, MA
    LEINART, AS
    YEDINAK, KC
    DISILVESTRO, RA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (06): : E688 - E694
  • [7] NUCLEAR ZINC UPTAKE AND INTERACTIONS AND METALLOTHIONEIN GENE-EXPRESSION ARE INFLUENCED BY DIETARY ZINC IN RATS
    COUSINS, RJ
    LEEAMBROSE, LM
    [J]. JOURNAL OF NUTRITION, 1992, 122 (01) : 56 - 64
  • [8] MEASUREMENT OF ZINC IN HEPATOCYTES BY USING A FLUORESCENT-PROBE, ZINQUIN - RELATIONSHIP TO METALLOTHIONEIN AND INTRACELLULAR ZINC
    COYLE, P
    ZALEWSKI, PD
    PHILCOX, JC
    FORBES, IJ
    WARD, AD
    LINCOLN, SF
    MAHADEVAN, I
    ROFE, AM
    [J]. BIOCHEMICAL JOURNAL, 1994, 303 : 781 - 786
  • [9] EVALUATION OF THE CD HEMOGLOBIN AFFINITY ASSAY FOR THE RAPID-DETERMINATION OF METALLOTHIONEIN IN BIOLOGICAL TISSUES
    EATON, DL
    TOAL, BF
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1982, 66 (01) : 134 - 142
  • [10] ETZEL KR, 1981, P SOC EXP BIOL MED, V167, P233