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饮食性锌缺乏症时 Wistar 大鼠肾和肺组织中 Zip-13mRNA 的过度表达。

Over-expression of Zip-13 mRNA in kidney and lung during dietary zinc deficiency in Wistar rats.

机构信息

Institute of Biochemistry and Molecular Biology, Shandong University School of Medicine, 44# Wenhua Xi Road, Jinan, 250012 Shandong, People's Republic of China.

出版信息

Mol Biol Rep. 2011 Mar;38(3):1869-74. doi: 10.1007/s11033-010-0304-y. Epub 2010 Sep 22.

DOI:10.1007/s11033-010-0304-y
PMID:20859692
Abstract

Zinc is an essential nutrient for all organisms, which is involved in the function of numerous key enzymes in metabolism. Two gene families have been identified involved in zinc homeostasis. ZnT transporters reduce intracellular zinc while Zip transporters increase intracellular zinc. Previous studies in our laboratory have shown that Zip-1, ZnT-1, Zip-2 and LIV-1 mRNA are associated with zinc level in established human breast cancer in nude mice model. In this study, six zinc transporters: ZnT-1, ZnT-2, ZnT-4, Zip-1, Zip-8 and Zip-13 were chosen. We aim to determine the relation between zinc transporters and zinc level in kidney and lung of Wistar rats. Eighteen Wistar rats were randomly divided into three groups: normal group, zinc-deficiency group and pair-fed group. After 22 days, the rats were killed and organs samples were taken, then zinc transporters mRNA were detected by RT-PCR. Compared with the normal group, Zip-13 shows an up-regulation (P < 0.05) in zinc-deficiency group both in kidney and lung, and Zip-8 was significantly lower (P < 0.05) in zinc-deficiency group in kidney.

摘要

锌是所有生物体必需的营养物质,参与代谢中许多关键酶的功能。已经确定了两个与锌稳态相关的基因家族。ZnT 转运蛋白降低细胞内锌含量,而 Zip 转运蛋白增加细胞内锌含量。我们实验室之前的研究表明,Zip-1、ZnT-1、Zip-2 和 LIV-1mRNA 与裸鼠模型中已建立的人乳腺癌中的锌水平相关。在这项研究中,选择了六种锌转运蛋白:ZnT-1、ZnT-2、ZnT-4、Zip-1、Zip-8 和 Zip-13。我们旨在确定肾脏和肺组织中锌转运蛋白与锌水平之间的关系。18 只 Wistar 大鼠随机分为三组:正常组、缺锌组和配对喂养组。22 天后,处死大鼠并采集器官样本,然后通过 RT-PCR 检测锌转运蛋白 mRNA。与正常组相比,缺锌组肾脏和肺部的 Zip-13 表达上调(P<0.05),而肾脏中 Zip-8 的表达显著降低(P<0.05)。

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本文引用的文献

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The role of zinc transporters in cadmium and manganese transport in mammalian cells.锌转运蛋白在哺乳动物细胞中镉和锰转运中的作用。
Biochimie. 2009 Oct;91(10):1218-22. doi: 10.1016/j.biochi.2009.04.002. Epub 2009 Apr 16.
2
The zinc transporter SLC39A13/ZIP13 is required for connective tissue development; its involvement in BMP/TGF-beta signaling pathways.锌转运蛋白SLC39A13/ZIP13是结缔组织发育所必需的;它参与骨形态发生蛋白/转化生长因子-β信号通路。
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Regulation of zinc transporters by dietary flaxseed lignan in human breast cancer xenografts.
Front Genet. 2018 Jan 31;8:234. doi: 10.3389/fgene.2017.00234. eCollection 2017.
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Mol Biol Rep. 2013 Aug;40(8):4979-84. doi: 10.1007/s11033-013-2598-z. Epub 2013 May 18.
膳食亚麻籽木脂素对人乳腺癌异种移植模型中锌转运体的调控作用
Mol Biol Rep. 2008 Dec;35(4):595-600. doi: 10.1007/s11033-007-9129-8. Epub 2007 Sep 5.
4
Regulation of zinc transporters by dietary zinc supplement in breast cancer.饮食锌补充剂对乳腺癌中锌转运蛋白的调节作用
Mol Biol Rep. 2007 Dec;34(4):241-7. doi: 10.1007/s11033-007-9082-6. Epub 2007 May 1.
5
Enhanced cadmium-induced testicular necrosis and renal proximal tubule damage caused by gene-dose increase in a Slc39a8-transgenic mouse line.在一个Slc39a8转基因小鼠品系中,基因剂量增加导致镉诱导的睾丸坏死和肾近端小管损伤加剧。
Am J Physiol Cell Physiol. 2007 Apr;292(4):C1523-35. doi: 10.1152/ajpcell.00409.2006. Epub 2006 Nov 15.
6
Identification of a mutation in SLC30A2 (ZnT-2) in women with low milk zinc concentration that results in transient neonatal zinc deficiency.在母乳锌浓度低的女性中鉴定出SLC30A2(锌转运体2)的一种突变,该突变导致短暂性新生儿锌缺乏。
J Biol Chem. 2006 Dec 22;281(51):39699-707. doi: 10.1074/jbc.M605821200. Epub 2006 Oct 25.
7
TGF-beta and epithelial-to-mesenchymal transitions.转化生长因子-β与上皮-间质转化
Oncogene. 2005 Aug 29;24(37):5764-74. doi: 10.1038/sj.onc.1208927.
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