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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >A comparison of DNA damage induced by aflatoxin B1 in hepatocyte-like cells, their progenitor mesenchymal stem cells and CD34(+) cells isolated from umbilical cord blood.
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A comparison of DNA damage induced by aflatoxin B1 in hepatocyte-like cells, their progenitor mesenchymal stem cells and CD34(+) cells isolated from umbilical cord blood.

机译:黄曲霉毒素B1诱导的肝样细胞,其祖细胞间充质干细胞和从脐带血中分离的CD34(+)细胞对DNA损伤的比较。

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摘要

This study compared the sensitivity of differentiated hepatocyte-like cells, their progenitor mesenchymal stem cells (MSCs) and CD34(+) stem cells to DNA damage and toxicity induced by aflatoxin B1 (AFB1). The hepatocyte-like cells and their progenitor cells (isolated from umbilical cord blood (UCB)) were each treated with AFB1 on day 15 of differentiation. Cell toxicity and genotoxicity effects were assessed using MTT and alkaline comet assays. AFB1 treatment resulted in a dose- and time-dependent inhibition of cell growth. The IC(50) values of AFB1 for hepatocytes differentiated from CD34(+) and MSCs were within the same range (44.7-46.8muM). The IC(50) calculated for non-differentiated MSCs and CD34(+) cells was slightly lower (42.0-43.4muM) than that calculated for their differentiated counterparts. However, the extent of DNA damage was different in differentiated and non-differentiated cells. The percentages of DNA (% DNA) in comet tails measured in hepatocytes differentiated from MSCs exposed to AFB1 (0, 2.5, 10 and 20muM) for 24h were approximately 15, 55, 65 and 70%, respectively. In comparison, hepatocytes from CD34(+) cells were more resistant to AFB1-induced DNA damage. Hepatocyte-MSCs were most sensitive to DNA damage, followed by UCB-CD34(+) cells, then UCB-MSCs and finally hepatocyte-CD34(+) cells. These results clearly showed that stem cells from different sources have different sensitivities to DNA damaging agents. These differences can be assigned to the expression levels of cytochrome P450 (CYP) particularly CYP3A4 in non-differentiated and differentiated cells. These data are useful in better understanding the susceptibility/resistance of stem cells in the process of differentiation to environmental toxicants.
机译:这项研究比较了分化的肝样细胞,其祖先间充质干细胞(MSCs)和CD34(+)干细胞对黄曲霉毒素B1(AFB1)诱导的DNA损伤和毒性的敏感性。在分化的第15天,分别用AFB1处理肝细胞样细胞及其祖细胞(从脐带血(UCB)分离)。使用MTT和碱彗星试验评估了细胞毒性和遗传毒性作用。 AFB1处理导致细胞生长的剂量和时间依赖性抑制。从CD34(+)和MSCs分化出的肝细胞AFB1的IC(50)值在同一范围内(44.7-46.8μM)。对于未分化的MSC和CD34(+)细胞,计算的IC(50)略低于针对分化的对应物计算的IC(50)(42.0-43.4μM)。但是,DNA损伤的程度在分化和未分化的细胞中是不同的。从暴露于AFB1(0、2.5、10和20μM)24小时的MSC分化而来的肝细胞中,彗尾中的DNA(%DNA)百分比分别约为15%,55%,65%和70%。相比之下,来自CD34(+)细胞的肝细胞对AFB1诱导的DNA损伤更具抵抗力。肝细胞-MSC对DNA损伤最敏感,其次是UCB-CD34(+)细胞,然后是UCB-MSC,最后是肝细胞-CD34(+)细胞。这些结果清楚地表明,不同来源的干细胞对DNA损伤剂的敏感性不同。这些差异可以归因于未分化和分化细胞中细胞色素P450(CYP)特别是CYP3A4的表达水平。这些数据有助于更好地了解干细胞在向环境有毒物质分化过程中的敏感性/抗性。

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