Department of Pediatric Urology Surgery, Children's Hospital of Chongqing Medical University, Chongqing, China.
Int J Toxicol. 2010 Mar-Apr;29(2):193-200. doi: 10.1177/1091581809355488.
This study investigated epigenetic (specifically, DNA methylation) changes and their impact on gene expression in testes induced by maternal exposure to Di-2-(ethylhexyl) phthalate (DEHP) in mice. Testicular dysgenesis syndrome was induced in fetuses and pups by maternal exposure to DEHP at 500 mg/kg/d, and testes were excised for analysis on gestation day (GD) 19 and postnatal days (PNDs) 3, 21, 56, and 90. High-performance liquid chromatography (HPLC) was performed to analyze DNA methylation status, and expression levels of the DNA methyltransferases were examined by quantitative real-time polymerase chain reaction (qPCR). Testis-specific gene, insulin-like hormone 3 (Insl3), and testosterone production were also detected. DEHP significantly increased DNA methylation levels on GD 19 and PND 3 (P < .05 and P < .05) but not on PNDs 21, 56, and 90. DEHP also significantly increased the expression of DNA methyltransferases. For DNA methyltransferase 1, the difference was not significant on PND 21, and DNA methyltransferase 3a and 3b returned to normal levels on PND 56. Fetal testes were a main target for DEHP as evidenced by a reduction in Insl3 expression and testosterone production. Effects of DEHP on Insl3 expression continued until PND 21. The DEHP-induced suppression of testosterone had not recovered on PND 56. Changes in DNA methylation may play an important role in abnormal testicular function caused by environmental factors such as maternal exposure to DEHP, which may be a mechanism of DEHP-mediated testicular toxicity.
本研究调查了母体暴露于邻苯二甲酸二(2-乙基己基)酯(DEHP)后小鼠睾丸中表观遗传(特别是 DNA 甲基化)变化及其对基因表达的影响。通过母体在妊娠第 19 天和产后第 3、21、56 和 90 天以 500mg/kg/d 的剂量暴露于 DEHP,诱导胎儿和幼仔的睾丸发育不良综合征,并切除睾丸进行分析。采用高效液相色谱法(HPLC)分析 DNA 甲基化状态,采用实时定量聚合酶链反应(qPCR)检测 DNA 甲基转移酶的表达水平。还检测了睾丸特异性基因胰岛素样激素 3(Insl3)和睾酮的产生。DEHP 显著增加了妊娠第 19 天和产后第 3 天(P <.05 和 P <.05)的 DNA 甲基化水平,但在产后第 21、56 和 90 天没有增加。DEHP 还显著增加了 DNA 甲基转移酶的表达。对于 DNA 甲基转移酶 1,在产后第 21 天差异不显著,而 DNA 甲基转移酶 3a 和 3b 在产后第 56 天恢复正常水平。胎儿睾丸是 DEHP 的主要靶标,表现为 Insl3 表达和睾酮产生减少。DEHP 对 Insl3 表达的影响持续到产后第 21 天。DEHP 诱导的睾酮抑制在产后第 56 天尚未恢复。DNA 甲基化的变化可能在母体暴露于 DEHP 等环境因素引起的睾丸功能异常中发挥重要作用,这可能是 DEHP 介导的睾丸毒性的一种机制。