首页> 外文期刊>The Journal of toxicological sciences >Long-term cadmium exposure enhances metallothionein-1 induction after subsequent exposure to high concentrations of cadmium in P1798 mouse lymphosarcoma cells
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Long-term cadmium exposure enhances metallothionein-1 induction after subsequent exposure to high concentrations of cadmium in P1798 mouse lymphosarcoma cells

机译:长期镉暴露在随后暴露于P1798小鼠淋巴瘤细胞中的高浓度镉后提高金属硫蛋白-1诱导

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摘要

Cadmium, a ubiquitous heavy metal, is a toxic industrial and environmental pollutant. The initial biological response to cadmium exposure is induction of metallothioneins (MTs), a family of cysteine-rich, low-molecular-weight proteins that bind primarily zinc, cadmium, or both. This MT induction protects against cadmium toxicity by quenching cadmium. However, the effects of long-term cadmium exposure on MT1 gene expression are largely unknown. To investigate these effects, we used P1798 mouse lymphosarcoma cells, in which the MT1 gene is suppressed. As previously reported, MT1 expression remained unchanged after cadmium treatment. However, MT1 induction was observed in cells treated with 0.1 mu M cadmium for 7 days, then exposed to 10 mu M cadmium for 3 hr. In cells treated with 0.1 mu M cadmium for 7 days, the transfected MT1 promoter reporter gene transcription and the cadmium incorporation in response to 10 mu M cadmium induction were similar to those in untreated P1798 cells. Bisulfite genomic sequencing revealed that 7 day treatment with 0.1 mu M cadmium slightly decreased CpG methylation in the 5' flanking region of the MT1 gene. Our results together show that cadmium treatment results in MT1 induction and epigenetic modification of the MT1 gene.
机译:镉,普遍存在的重金属,是有毒的工业和环境污染物。对镉暴露的初始生物反应是诱导金属噻吩(MTS),一种富含锌,镉或两者的半胱氨酸的富含低分子量蛋白质。该MT诱导通过淬火镉防止镉毒性。然而,长期镉暴露对MT1基因表达的影响主要是未知的。为了研究这些效果,我们使用了P1798小鼠淋巴瘤细胞,其中抑制了MT1基因。如前所述,在镉处理后,MT1表达保持不变。然而,在用0.1μm镉处理7天处理的细胞中观察到MT1诱导,然后暴露于10μm镉3小时。在用0.1μm镉处理7天处理的细胞中,转染的MT1启动子报告基因转录和镉掺入响应于10μM镉诱导与未处理的P1798细胞中的相似。亚硫酸氢盐基因组测序显示,在MT1基因的5'侧翼区域中略微降低了0.1μm镉的7天处理。我们的结果在一起表明镉治疗导致MT1诱导和MT1基因的表观遗传修饰。

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