Svoboda Laurie K, Wang Kai, Cavalcante Raymond G, Neier Kari, Colacino Justin A, Sartor Maureen A, Dolinoy Dana C
Environmental Health Sciences, School of Public Health, University of Michigan, Ann Arbor, MI, USA.
Department of Computational Medicine and Bioinformatics, Medical School, University of Michigan, Ann Arbor, MI, USA.
Epigenet Insights. 2020 Aug 5;13:2516865720939971. doi: 10.1177/2516865720939971. eCollection 2020.
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.
邻苯二甲酸酯类增塑剂是普遍存在的化学物质,在动物模型和人类中与多种心血管疾病有关。尽管如此,邻苯二甲酸酯暴露导致不良心脏健康结果的机制尚不清楚。特别是,孕期邻苯二甲酸酯暴露是否会干扰心血管系统的正常发育编程,以及这可能对长期疾病风险产生的影响,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具有性别特异性。然而,性别对心脏对邻苯二甲酸酯暴露易感性的影响尚未得到研究。发育暴露可能影响长期健康的一种机制是通过改变DNA甲基化编程。在这项研究中,我们利用一个已建立的与人类相关的围产期暴露小鼠模型和增强的简化代表性亚硫酸氢盐测序技术,来研究邻苯二甲酸二(2-乙基己基)酯(DEHP)暴露对5月龄成年雄性和雌性后代心脏DNA甲基化的长期影响(每个性别和暴露组有5-7只小鼠)。围产期DEHP暴露导致心脏中数百个性别特异性的差异甲基化胞嘧啶(DMC)和差异甲基化区域(DMR)。对DMC的通路分析显示,女性中有几个通路富集,包括胰岛素信号传导、组蛋白甲基化调节和酪氨酸磷酸酶活性。在男性中,DMC在葡萄糖转运、能量生成和发育程序方面富集。值得注意的是,在我们的小鼠模型中,许多因DEHP暴露而差异甲基化的性别特异性基因,在从人类心力衰竭患者收集的心脏组织的已发表数据中也存在差异甲基化。总之,这些数据突出了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的一个生物学变量的重要性。