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新生大鼠卵巢镉暴露诱导原始卵泡发育障碍及SCF/c-kit基因的差异表达。

Cadmium exposure in newborn rats ovary induces developmental disorders of primordial follicles and the differential expression of SCF/c-kit gene.

作者信息

Zhang Wenchang, Wu Tingting, Zhang Chenyun, Luo Lingfeng, Xie Meimei, Huang Huiling

机构信息

Fujian Provincial Key Laboratory of Environment factors and Cancer, Key Laboratory of Environment and Health, School of Public Health, Fujian Medical University, Xueyuan Road No.1, Minhou County, Fuzhou 350108 China.

Fujian Center for Disease Control and Prevention, No.76 Jintai Road, Fuzhou, Fujian, 350001, China.

出版信息

Toxicol Lett. 2017 Oct 5;280:20-28. doi: 10.1016/j.toxlet.2017.08.004. Epub 2017 Aug 9.

Abstract

Since the 1990s, the rising problem that gonad reproductive toxicity on adult female after exposing to cadmium (Cd), an environmental endocrine disruptor, has attracted high attention at home and abroad,and was systematically studied. Our research focuses on a further problem is that early cadmium exposure (during birth to before puberty) impact on development and function of ovarian cells and its possible mechanism. Our research focuses on the changes of ovarian cells growth and development after the newborn rat ovaries with cadmium exposure in vitro, and different expression of ovarian cells development-related factors, SCF/c-kit and changes of their DNA methylation status. We obtained ovaries from 4-day-old SD rats and cultured them in DMEM/F12 mixed with α-MEM media in vitro. Different doses of cadmium were designed as control, 0.5, 5, 10 and 50μM, and then the constituent ratio of ovarian follicle and follicular oocytes diameter were observed with microscope after 4-h exposure. We found that the increased constituent ratio of original follicle and decreased diameter of all levels of follicular oocytes(compared with control, with statistically significant differences, P<0.01).After the measurement of expression of SCF/c-kit by qRT-PCR and Western Blotting, the mRNA and protein expression of SCF/c-kit in ovarian were both decreased. We further found that the increased constituent ratio of growth follicle and increased diameter of oocytes under the treatment of adding SCF in cell culture media. Finally, MALDI-TOF-MS method showed DNA-low methylation status of SCF/c-kit promoter region after Cd exposure. Overall, we concluded that the exposure of cadimium (5-50μM) on newborn rats ovaries could inhibit follicle development.SCF/c-kit system might mediate follicle development damage caused by cadmium, which is associated with DNA hypomethylation of SCF/c-kit promoter region may be worthy of further study.

摘要

自20世纪90年代以来,环境内分泌干扰物镉(Cd)对成年雌性性腺生殖毒性这一日益严重的问题已引起国内外高度关注,并得到了系统研究。我们的研究进一步聚焦于早期镉暴露(出生至青春期前)对卵巢细胞发育和功能的影响及其可能机制。我们的研究重点是新生大鼠卵巢体外镉暴露后卵巢细胞生长发育的变化、卵巢细胞发育相关因子SCF/c-kit的不同表达及其DNA甲基化状态的改变。我们从4日龄的SD大鼠获取卵巢,在体外将其培养于DMEM/F12与α-MEM混合培养基中。设计不同剂量的镉作为对照,分别为0.5、5、10和50μM,4小时暴露后用显微镜观察卵巢卵泡组成比例和卵泡卵母细胞直径。我们发现原始卵泡组成比例增加,各级卵泡卵母细胞直径减小(与对照组相比,差异有统计学意义,P<0.01)。通过qRT-PCR和蛋白质免疫印迹法检测SCF/c-kit的表达后,发现卵巢中SCF/c-kit的mRNA和蛋白表达均降低。我们进一步发现,在细胞培养基中添加SCF处理后,生长卵泡组成比例增加,卵母细胞直径增大。最后,基质辅助激光解吸电离飞行时间质谱法显示镉暴露后SCF/c-kit启动子区域DNA低甲基化状态。总体而言,我们得出结论,镉(5-50μM)暴露于新生大鼠卵巢可抑制卵泡发育。SCF/c-kit系统可能介导镉所致卵泡发育损伤,这与SCF/c-kit启动子区域DNA低甲基化有关,可能值得进一步研究。

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