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人黄素化壁颗粒细胞在体暴露于邻苯二甲酸二丁酯影响全局基因表达。

In Vitro Exposure of Human Luteinized Mural Granulosa Cells to Dibutyl Phthalate Affects Global Gene Expression.

机构信息

Infertility and IVF Unit, Department of Obstetrics and Gynecology, Chaim Sheba Medical Center, Tel Hashomer and Sackler School of Medicine, Tel-Aviv University, Israel.

Department of Molecular Biology, Ariel University, Ariel 40700, Israel.

出版信息

Toxicol Sci. 2017 Nov 1;160(1):180-188. doi: 10.1093/toxsci/kfx170.

Abstract

Exposure to dibutyl phthalate (DBP) is ubiquitous among women of reproductive age. Previous studies in animal models and in human cells in vitro have shown that exposure to DBP disrupts ovarian function. Here, we examined the effect of DBP on global gene expression in mural granulosa cells (MGCs) in vitro. Primary cultures of MGC obtained from 48 patients undergoing IVF were treated with increasing concentrations of DBP (0, 0.01, 0.1, 1, 10, or 100 µg/ml) for 48 h. Microarray analysis was used to identify genes exhibiting expression changes following DBP exposure. When compared with untreated cells, exposure to 100 µg/ml DBP resulted in significant differences in expression of 346 annotated genes (> 2-fold; q value < .05). Of them, 151 were upregulated and 195 downregulated. The main functional annotations affected by DBP were associated with cell cycle, mitosis, Rho GTPases, PLK1, Aurora B signaling pathways, and E2F-mediated regulation of DNA replication. No significant differences in gene expression were observed for the lower concentrations of DBP (0.01, 0.1, 1, and 10 µg/ml) compared with controls for both the microarray analysis and genes validated by quantitative real-time (qRT)-PCR. This study provides important molecular inputs on the effect of short-term DBP exposure on human MGCs in vitro. Our results indicate that acute treatment with high concentrations of DBP alters gene expression pathways mainly associated with the cell cycle.

摘要

二丁基邻苯二甲酸酯(DBP)暴露在育龄妇女中普遍存在。以前的动物模型和体外人细胞研究表明,DBP 暴露会破坏卵巢功能。在这里,我们研究了 DBP 对体外壁颗粒细胞(MGC)中整体基因表达的影响。从接受 IVF 的 48 名患者中获得的 MGC 原代培养物,用递增浓度的 DBP(0、0.01、0.1、1、10 或 100μg/ml)处理 48 小时。微阵列分析用于鉴定 DBP 暴露后表达发生变化的基因。与未处理的细胞相比,100μg/ml DBP 暴露导致 346 个注释基因(>2 倍;q 值<.05)的表达显著差异。其中,151 个上调,195 个下调。受 DBP 影响的主要功能注释与细胞周期、有丝分裂、Rho GTPases、PLK1、Aurora B 信号通路和 E2F 介导的 DNA 复制调控有关。与对照相比,较低浓度的 DBP(0.01、0.1、1 和 10μg/ml)对微阵列分析和通过定量实时(qRT)-PCR 验证的基因均未观察到基因表达的显著差异。这项研究为 DBP 对体外人 MGC 的短期暴露的影响提供了重要的分子输入。我们的结果表明,急性高浓度 DBP 处理会改变主要与细胞周期相关的基因表达途径。

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