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The Role of miR-34a in Tritiated Water Toxicity in Human Umbilical Vein Endothelial Cells

机译:miR-34a在人脐静脉内皮细胞Tri水毒性中的作用

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In this work, we investigated the toxic effects of tritiated water (HTO) on the cardiovascular system. We examined the role of microRNA-34a (miR-34a) in DNA damage and repair in human umbilical vein endothelial cells (HUVECs) exposed to HTO. Cell proliferation capacity was evaluated by cell counting, and miR-34a expression was detected using quantitative PCR (QT-PCR). The Comet assay and -H2AX immunostaining were used to measure DNA double-strand breaks (DSBs). Reverse transcription polymerase chain reaction was used to measure the expression level of c-myc messenger RNA (mRNA). The cells exposed to HTO showed significantly lower proliferation than the control cells over 3 days. The DNA damage in the HTO group was more severe than that in the control group, at each time point examined. The expression of miR-34a mimics caused increased DNA DSBs whereas that of the miR-34a inhibitor caused decreased DNA DSBs. The proliferation viability was the opposite for the miR-34a mimics and inhibitor groups. The expression levels of c-myc mRNA in cells transfected with miR-34a mimics were lower than that in cells transfected with the miR-34a-5p inhibitor, at 0.5 hours and 2 hours after transfection. In summary, miR-34a mediates HTO toxicity in HUVECs by downregulating the expression of c-myc.
机译:在这项工作中,我们研究了of水(HTO)对心血管系统的毒性作用。我们检查了microRNA-34a(miR-34a)在暴露于HTO的人脐静脉内皮细胞(HUVEC)中的DNA损伤和修复中的作用。通过细胞计数评估细胞增殖能力,并使用定量PCR(QT-PCR)检测miR-34a表达。 Comet分析和-H2AX免疫染色用于测量DNA双链断裂(DSB)。逆转录聚合酶链反应用于测量c-myc信使RNA(mRNA)的表达水平。暴露于HTO的细胞在3天内显示出比对照细胞低得多的增殖。在每个检查时间点,HTO组的DNA损伤都比对照组严重。 miR-34a模拟物的表达引起DNA DSB增加,而miR-34a抑制剂的表达引起DNA DSB减少。对于miR-34a模拟物和抑制剂组,增殖能力相反。在转染后0.5小时和2小时,用miR-34a模拟物转染的细胞中c-myc mRNA的表达水平低于用miR-34a-5p抑制剂转染的细胞。总之,miR-34a通过下调c-myc的表达介导HUVEC的HTO毒性。

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