发育性邻苯二甲酸盐暴露对心脏DNA甲基化的性别特异性编程。

IF 3.2 Q2 GENETICS & HEREDITY Epigenetics Insights Pub Date : 2020-08-05 eCollection Date: 2020-01-01 DOI:10.1177/2516865720939971
Laurie K Svoboda, Kai Wang, Raymond G Cavalcante, Kari Neier, Justin A Colacino, Maureen A Sartor, Dana C Dolinoy
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引用次数: 13

摘要

邻苯二甲酸酯增塑剂是一种普遍存在的化学物质,与动物模型和人类的几种心血管疾病有关。尽管如此,邻苯二甲酸盐暴露导致不良心脏健康结果的机制尚不清楚。特别是,怀孕期间接触邻苯二甲酸盐是否会干扰心血管系统的正常发育,以及由此产生的对长期疾病风险的影响,目前尚不清楚。最近的研究表明,邻苯二甲酸酯对代谢和神经行为结果的影响是性别特异性的。然而,性别对邻苯二甲酸盐暴露的心脏易感性的影响尚未调查。发育暴露可能影响长期健康的一种机制是通过改变DNA甲基化程序。在这项工作中,我们利用已建立的与人类相关的围产期暴露小鼠模型和增强的亚硫酸盐还原测序来研究邻苯二甲酸二乙基己基酯(DEHP)暴露对5个月大成年雄性和雌性后代心脏DNA甲基化的长期影响(n = 5-7只小鼠,每性别和暴露)。围产期DEHP暴露导致心脏中数百个性别特异性、差异甲基化的胞嘧啶(DMCs)和差异甲基化区域(DMRs)。DMCs的通路分析显示,雌性DMCs在几个通路中富集,包括胰岛素信号、组蛋白甲基化调节和酪氨酸磷酸酶活性。在雄性中,DMCs被富集用于葡萄糖运输、能量产生和发育程序。值得注意的是,在我们的小鼠模型中,许多性别特异性基因在DEHP暴露中差异甲基化,在从人类心力衰竭患者收集的心脏组织的公开数据中也存在差异甲基化。总之,这些数据强调了DNA甲基化在dehp诱导的心脏效应中的潜在作用,并强调了性别作为环境健康研究中生物变量的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Sex-Specific Programming of Cardiac DNA Methylation by Developmental Phthalate Exposure.

Phthalate plasticizers are ubiquitous chemicals linked to several cardiovascular diseases in animal models and humans. Despite this, the mechanisms by which phthalate exposures cause adverse cardiac health outcomes are unclear. In particular, whether phthalate exposures during pregnancy interfere with normal developmental programming of the cardiovascular system, and the resulting implications this may have for long-term disease risk, are unknown. Recent studies suggest that the effects of phthalates on metabolic and neurobehavioral outcomes are sex-specific. However, the influence of sex on cardiac susceptibility to phthalate exposures has not been investigated. One mechanism by which developmental exposures may influence long-term health is through altered programming of DNA methylation. In this work, we utilized an established mouse model of human-relevant perinatal exposure and enhanced reduced representation bisulfite sequencing to investigate the long-term effects of diethylhexyl phthalate (DEHP) exposure on DNA methylation in the hearts of adult male and female offspring at 5 months of age (n = 5-7 mice per sex and exposure). Perinatal DEHP exposure led to hundreds of sex-specific, differentially methylated cytosines (DMCs) and differentially methylated regions (DMRs) in the heart. Pathway analysis of DMCs revealed enrichment for several pathways in females, including insulin signaling, regulation of histone methylation, and tyrosine phosphatase activity. In males, DMCs were enriched for glucose transport, energy generation, and developmental programs. Notably, many sex-specific genes differentially methylated with DEHP exposure in our mouse model were also differentially methylated in published data of heart tissues collected from human heart failure patients. Together, these data highlight the potential role for DNA methylation in DEHP-induced cardiac effects and emphasize the importance of sex as a biological variable in environmental health studies.

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来源期刊
Epigenetics Insights
Epigenetics Insights GENETICS & HEREDITY-
CiteScore
5.10
自引率
0.00%
发文量
10
审稿时长
8 weeks
期刊最新文献
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