Kradolfer David, Flöter Veronika L, Bick Jochen T, Fürst Rainer W, Rode Kristina, Brehm Ralph, Henning Heiko, Waberski Dagmar, Bauersachs Stefan, Ulbrich Susanne E
ETH Zurich, Animal Physiology, Institute of Agricultural Sciences, Zurich, Switzerland.
Technische Universität München, Physiology Weihenstephan, Freising, Germany.
Mol Cell Endocrinol. 2016 Jul 15;430:125-37. doi: 10.1016/j.mce.2016.04.005. Epub 2016 Apr 7.
There is growing evidence that early life exposure to endocrine disrupting chemicals might increase the risk for certain adult onset diseases, in particular reproductive health problems and hormone dependent cancers. Studies in rodents suggest that perinatal exposure to even low doses of estrogenic substances can cause adverse effects, including epigenetic reprogramming of the prostate and increased formation of precancerous lesions. We analyzed the effects of an in utero exposure to the strongest natural estrogen, estradiol-17β, in a pig model. Two different low and one high dose of estradiol-17β (0.05, 10 and 1000 μg/kg body weight/day) were orally applied to gilts during pregnancy and potential effects on the reproductive system of the offspring were analyzed. No significant effects on sperm vitality parameters and testes size were observed in adult boars. However, prenatal exposure to the high dose decreased absolute, but not relative weight of the testes in prepubertal piglets. RNA sequencing revealed significantly regulated genes of the prepubertal prostate, while testes and uteri were not affected. Notably, we found an increased prostate expression of CCDC80 and a decreased ADH1C expression in the low dose treatment groups. BGN and SPARC, two genes associated with prostate tumor progression, were as well more abundant in exposed animals. Strikingly, the gene body DNA methylation level of BGN was accordingly increased in the high dose group. Thus, while only prenatal exposure to a high dose of estrogen altered testes development and local DNA methylation of the prostate, even low dose exposure had significant effects on gene expression in the prostate of prepubertal piglet offspring. The relevance of these distinct, but subtle transcriptional changes following low dose treatment lacking a clear phenotype calls for further long-term investigations. An epigenetic reprogramming of the pig prostate due to prenatal estrogen cannot be neglected.
越来越多的证据表明,早年接触内分泌干扰化学物质可能会增加某些成年后发病疾病的风险,尤其是生殖健康问题和激素依赖性癌症。对啮齿动物的研究表明,围产期接触即使低剂量的雌激素物质也会产生不良影响,包括前列腺的表观遗传重编程和癌前病变形成增加。我们在猪模型中分析了子宫内暴露于最强的天然雌激素17β-雌二醇的影响。在妊娠期间对后备母猪口服两种不同的低剂量和一种高剂量的17β-雌二醇(0.05、10和1000μg/千克体重/天),并分析对后代生殖系统的潜在影响。在成年公猪中未观察到对精子活力参数和睾丸大小的显著影响。然而,产前暴露于高剂量会降低青春期前仔猪睾丸的绝对重量,但不影响相对重量。RNA测序显示青春期前前列腺的基因有显著调控,而睾丸和子宫未受影响。值得注意的是,我们发现在低剂量治疗组中CCDC80在前列腺中的表达增加,而ADH1C的表达降低。与前列腺肿瘤进展相关的两个基因BGN和SPARC在暴露动物中也更为丰富。引人注目的是,高剂量组中BGN的基因体DNA甲基化水平相应增加。因此,虽然只有产前暴露于高剂量雌激素会改变睾丸发育和前列腺的局部DNA甲基化,但即使低剂量暴露也会对青春期前仔猪后代前列腺中的基因表达产生显著影响。低剂量治疗后这些明显但细微的转录变化缺乏明确的表型,其相关性需要进一步的长期研究。产前雌激素导致猪前列腺的表观遗传重编程不容忽视。