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从断奶到成熟持续接触镉会导致卵巢卵泡发育相关的 SCF/c-kit 基因表达下调,以及相应的 DNA 甲基化/miRNA 模式变化。

Continuous cadmium exposure from weaning to maturity induces downregulation of ovarian follicle development-related SCF/c-kit gene expression and the corresponding changes of DNA methylation/microRNA pattern.

机构信息

Key Laboratory of Environment and Health, Fujian Medical University, Fuzhou 350004, China.

Pharmacy Department, Fujian Health College, Fuzhou 350004, China.

出版信息

Toxicol Lett. 2014 Mar 21;225(3):367-77. doi: 10.1016/j.toxlet.2014.01.012. Epub 2014 Jan 21.

DOI:10.1016/j.toxlet.2014.01.012
PMID:24462979
Abstract

Cadmium (Cd) impairs ovary structure and function in mature animals. However, the influence of Cd on follicle development from weaning to maturity is obscure. In the current study, 21-day-old Wistar rats were administered Cd chloride at doses of 0, 0.5, 2.0 and 8.0 mg/kg body weight once a day for eight weeks by gavage. After administration, a significant decrease in ovarian wet weight, ovarian/body weight ratios, and primordial follicles, in addition to an increase in atresic follicles, were observed. Transmission electron microscopy and TUNEL assay confirmed the increase of follicle apoptosis as Cd concentration increased. Real-time quantitative PCR and Western blotting showed a significantly decreased expression of follicle development-related factors, stem cell factor (SCF) and c-kit. Bisulfite sequencing suggested that the total methylation percentages of SCF/c-kit promoter region were not obvious change after Cd exposure. Real-time quantitative PCR revealed a significantly increased expression of miR-193, miR-221 and miR-222, which regulate c-kit, in the 2.0 mg/kg and 8.0 mg/kg treatment groups. Overall, this study proved that Cd administration from weaning to maturity could damage follicle development, suggesting that SCF/c-kit might play an important role in this effect. In addition, microRNAs might play a role in c-kit protein downregulation.

摘要

镉 (Cd) 会损害成熟动物的卵巢结构和功能。然而,Cd 对从断奶到成熟的卵泡发育的影响尚不清楚。在本研究中,21 日龄 Wistar 大鼠通过灌胃每天给予氯化镉 0、0.5、2.0 和 8.0mg/kg 体重,连续 8 周。给药后,卵巢湿重、卵巢/体重比和原始卵泡显著减少,闭锁卵泡增加。透射电子显微镜和 TUNEL 检测证实,随着 Cd 浓度的增加,卵泡凋亡增加。实时定量 PCR 和 Western blot 显示,与卵泡发育相关的因子,干细胞因子 (SCF) 和 c-kit 的表达显著降低。亚硫酸氢盐测序表明,Cd 暴露后 SCF/c-kit 启动子区域的总甲基化百分比没有明显变化。实时定量 PCR 显示,在 2.0mg/kg 和 8.0mg/kg 处理组中,调节 c-kit 的 miR-193、miR-221 和 miR-222 的表达显著增加。总之,这项研究证明,从断奶到成熟期间给予 Cd 会损害卵泡发育,提示 SCF/c-kit 可能在这种作用中发挥重要作用。此外,microRNAs 可能在 c-kit 蛋白下调中发挥作用。

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