Differential regulation of zinc efflux transporters ZnT-1, ZnT-5 and ZnT-7 gene expression by zinc levels: a real-time RT-PCR study

被引:72
|
作者
Devergnas, S
Chimienti, F
Naud, N
Pennequin, A
Coquerel, Y
Chantegrel, J
Favier, A
Seve, M
机构
[1] CEA, Lab Les Acides Nucl, DRFMC, SCIB,LAN, F-38000 Grenoble, France
[2] CRSSA, Dept Radiobiol & Radiopathol, F-38700 La Tronche, France
[3] Ctr Univ St Jerome, Lab ReSO, UMR, CNRS,SYMBIO, F-13000 Marseille, France
关键词
ZnT; zinc transporter; zinc chelation; gene expression; real-time PCR;
D O I
10.1016/j.bcp.2004.05.024
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Intracellular zinc levels are strictly regulated by zinc channels and zinc-binding proteins to maintain cellular zinc-dependent functions. We demonstrated a correlation between extracellular zinc concentration and intracellular exchangeable zinc levels using the fluorescent zinc-specific probes zinquin and zinpyr-1. The effect of extracellular zinc status on the regulation of the two trans-Golgi network directed zinc transporters ZnT-5 and ZnT-7 was next studied by real-time RT-PCR in zinc supplemented or depleted HeLa cells. While sub-toxic extracellular zinc addition strongly induced the efflux transporter ZnT-1 gene expression, consistent with its activation by the transcription factor MTF-1, treated HeLa cells did not display any change in ZnT-5 and ZnT-7 mRNA levels compared to control cells. In contrast, zinc depletion induced by non-toxic doses of the zinc chelator TPEN (N,N,N',N' tetrakis-(2 pyridylmethyl) ethylene diamine) resulted in a up to eight-fold induction of transporters ZnT-5 and ZnT-7 mRNA levels, providing the first evidence of a transcriptional control of these two zinc efflux transporters by zinc deficiency in cultured cells. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:699 / 709
页数:11
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