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慢性镉暴露的肺上皮细胞中锌转运体Zip8(Slc39a8)的渐进性沉默

Progressive silencing of the zinc transporter Zip8 (Slc39a8) in chronic cadmium-exposed lung epithelial cells.

作者信息

Gao Yangmin, Xu Yanming, Wu Dandan, Yu Feiyuan, Yang Lei, Yao Yue, Liang Zhanling, Lau Andy T Y

机构信息

Laboratory of Cancer Biology and Epigenetics, Department of Cell Biology and Genetics, Shantou University Medical College, Shantou 515041, China.

出版信息

Acta Biochim Biophys Sin (Shanghai). 2017 May 1;49(5):444-449. doi: 10.1093/abbs/gmx022.

Abstract

Cadmium (Cd), a non-essential metal, stealthily enters the cells by utilizing the essential metal importing pathways. The zinc transporters Zip8, Zip14, and divalent metal transporter 1 (Dmt1) are now emerging as several important metal transporters involved in cellular Cd incorporation and their expressions have been shown to be down-regulated in several Cd-resistant (CdR) cell lines, however, the involvement of these transporters during the development of Cd-resistance in lung cells is unclear. In this study, we therefore check the expression of these metal transporters in our previously established rat lung epithelial cells (LECs) and show that the level of Zip8 is progressively silenced when LECs are adapted to increasing concentrations of CdCl2 (from 1 to 20 μM). Subsequent measurement of the cellular Cd content indicated that CdR LECs exhibit a marked decrease of Cd accumulation, possibly due to the loss of Zip8 expression. We investigate the possibility that epigenetic silencing of the Zip8 gene by DNA hypermethylation is involved in the down-regulation of Zip8 expression. CdR LECs show a higher mRNA level of DNA methyltransferase 3b (Dnmt3b) than parental cells. Treatment of CdR LECs with 5-aza-2'-deoxycytidine, an inhibitor of DNA methyltransferases, reverted the expression of Zip8 and sensitivity to Cd in these cells, indicating the critical role of Zip8 for Cd import. Taken together, our results demonstrate that the progressive silencing of Zip8 expression is involved in the acquisition of resistance against Cd in lung cells, representing an adaptive survival mechanism that resists Cd-induced cytotoxicity.

摘要

镉(Cd)是一种非必需金属,它通过利用必需金属的导入途径悄悄进入细胞。锌转运蛋白Zip8、Zip14和二价金属转运蛋白1(Dmt1)正逐渐成为参与细胞镉摄取的几种重要金属转运蛋白,并且它们的表达在几种镉抗性(CdR)细胞系中已显示下调,然而,这些转运蛋白在肺细胞镉抗性发展过程中的作用尚不清楚。因此,在本研究中,我们检测了这些金属转运蛋白在我们先前建立的大鼠肺上皮细胞(LEC)中的表达,结果表明,当LEC适应浓度不断增加的氯化镉(从1到20 μM)时,Zip8的水平逐渐沉默。随后对细胞镉含量的测量表明,CdR LEC中镉积累显著减少,这可能是由于Zip8表达缺失所致。我们研究了DNA高甲基化导致Zip8基因表观遗传沉默参与Zip8表达下调的可能性。CdR LEC显示出比亲代细胞更高的DNA甲基转移酶3b(Dnmt3b)mRNA水平。用DNA甲基转移酶抑制剂5-氮杂-2'-脱氧胞苷处理CdR LEC,可使这些细胞中Zip8的表达和对镉的敏感性恢复,表明Zip8对镉导入起关键作用。综上所述,我们的结果表明,Zip8表达的逐渐沉默参与了肺细胞对镉抗性的获得,代表了一种抵抗镉诱导细胞毒性的适应性生存机制。

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