邻苯二甲酸二乙酯与胎儿大脑发育的可能相互作用

R. Hokanson, R. Chowdhary, D. Busbee
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引用次数: 0

摘要

许多天然和合成化合物,包括用作增塑剂或用于化妆品生产和治疗的各种化学品,具有类固醇激动剂或拮抗剂活性,改变激素调节的基因表达。广泛用作增塑剂和消费品的邻苯二甲酸二乙酯(二乙基邻苯二甲酸二酯)使用人类肾上皮细胞系293T/17进行了评估。研究的重点是中枢神经系统发育或功能所必需的基因。分别用1、10或100 μM邻苯二甲酸盐处理细胞,检测处理细胞中的基因表达,结果显示,与未处理细胞相比,处理细胞中大量基因显著上调或下调。在使用的DNA阵列芯片上的19,000个人类基因中,选择两个特定基因FGD1和NGPF2,使用定量实时PCR (qrtPCR)数据来证实mRNA水平,以确认从微阵列检测中获得的结果。FGD1(面部生殖发育不良)和NGPF2(神经突生长促进因子2,也称为Midkine, MDK)显示出胎儿大脑发育必需基因的显著下调,可能是雌激素协同作用。这些研究旨在提供广泛分布的化学物质邻苯二甲酸二乙酯(DEP)基因表达改变能力的数据,并显示先前报道的广泛存在的DEP与参考人群尿液样本中DEP的禁忌物MEP之间的可能联系,体外人类细胞中基因表达改变的可能性,以及可能与子宫内暴露于DEP相关的神经发育影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diethylphthalate, Possible Interactions in Fetal Brain Development
Many natural and synthetic compounds, including a variety of the chemicals used as plasticizers or in the pro- duction of cosmetics and therapeutics, have steroid agonist or antagonist activities, altering hormone-regulated gene ex- pression. The phthalate (diethylphthalate, extensively used as a plasticizer and in consumer products, are evaluated using the human renal epithelial cell line 293T/17. Emphasis of the study was on genes essential for central nervous system de- velopment or function. Cells were treated with 1, 10 or 100 μM phthalate and gene expression was measured in treated cells, showing significant up- or down-regulation of a large number of genes in treated compared to untreated cells. Of the 19,000 human genes on the DNA array chip utilized, two specific genes, FGD1 and NGPF2, were selected to corroborate mRNA levels using quantitative real time PCR (qrtPCR) data to confirm results obtained from the microarray determina- tions. FGD1 (faciogenital dysplasia) and NGPF2 (neurite growth-promoting factor 2, also called Midkine, MDK), showed a significant, possibly estrogen-synergistic, down-regulation of genes essential for fetal brain development. These studies were designed to provide data on the gene expression-altering capacity of a widely distributed chemical, diethylphthalate (DEP), and to show possible associations between the previously reported widespread presence of DEP and the DEP me- tabolite, MEP, in urine samples from a reference population, the potential for altered gene expression in human cells in vi- tro, and possible neurodevelopmental effects that could be correlated with in utero exposure to DEP.
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