Ni2+ transport by the human Na+/Ca2+ exchanger expressed in Sf9 cells

被引:7
作者
Egger, M
Ruknudin, A
Niggli, E
Lederer, WJ
Schulze, DH
机构
[1] Univ Maryland, Dept Microbiol & Immunol, Sch Med, Baltimore, MD 21201 USA
[2] Univ Bern, Dept Physiol, CH-3012 Bern, Switzerland
[3] Univ Maryland, Inst Biotechnol, Baltimore, MD 21201 USA
[4] Univ Maryland, Dept Physiol, Baltimore, MD 21201 USA
[5] Univ Maryland, Dept Mol Biol & Biophys, Baltimore, MD 21201 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1999年 / 276卷 / 05期
关键词
heart; nickel ion quench; fluo; 3;
D O I
10.1152/ajpcell.1999.276.5.C1184
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mechanism of Ni2+ block of the Na+/Ca2+ exchanger was examined in Sf9 cells expressing the human heart Na+/Ca2+ exchanger (NCX1-NACA1). As predicted from the reported actions of Ni2+, its application reduced extracellular Na+-dependent changes in intracellular Ca2+ concentration (measured by flue 3 fluorescence changes). However, contrary to expectation, the reduced fluorescence was accompanied by measured Ni-63(2+) entry. The Ni-63(2+) entry was observed in Sf9 cells expressing the Na+/Ca2+ exchanger but not in control cells. The established sequential transport mechanism of the Na+/Ca2+ exchanger could be compatible with these results if one of the two ion translocation steps is blocked by Ni2+ and the other permits Ni2+ translocation. We conclude that, because Ni2+ entry was inhibited by extracellular Ca2+ and enhanced by extracellular Na+, the Ca2+ translocation step moved Ni2+, whereas the Na+ translocation step was inhibited by Ni2+. A model is presented to discuss these findings.
引用
收藏
页码:C1184 / C1192
页数:9
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