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

机译:通过发育邻苯二甲酸盐暴露的心脏DNA甲基化的性别特异性编程

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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.
机译:邻苯二甲酸酯增塑剂是普遍存在的化学品,与动物模型和人类的几种心血管疾病有关。尽管如此,邻苯二甲酸盐暴露会导致不良心脏健康结果的机制尚不清楚。特别地,妊娠期间的邻苯二甲酸酯暴露是否干扰心血管系统的正常发育规划,并且这可能具有长期疾病风险的产生含义,是未知的。最近的研究表明,邻苯二甲酸酯对代谢和神经兽性结果的影响是性别特异性的。然而,尚未研究性对性对心脏敏感性对邻苯二甲酸盐暴露的影响。发育暴露可能影响长期健康的一种机制是通过改变DNA甲基化的编程。在这项工作中,我们利用了近期人类相关的围产量暴露的鼠标模型,并增强了伯硫酸氢盐测序的增强,研究了邻苯二甲酸二乙酯(DEHP)暴露于成年男性和女性后代的DNA甲基化的长期影响?几个月的年龄(n?=?5-7个老鼠每当性和曝光)。围产期Dehp暴露导致数百种异性,差异甲基化胞嘧啶(DMC)和心脏差异甲基化区域(DMRS)。 DMC的途径分析显示了女性的几种途径的富集,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。在雄性中,DMC富集为葡萄糖运输,能量产生和发展方案。值得注意的是,在我们的小鼠模型中差异甲基化的许多性特异性基因在我们的小鼠模型中差异甲基化,在来自人心力衰竭患者收集的心脏组织的公开数据中也差异甲基化。这些数据在一起突出了DNA甲基化在DeHP诱导的心脏作用中的潜在作用,并强调性行为环境健康研究中的生物变量。

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