Shen Yu-Ting, Song Yue-Qiang, He Xiao-Qin, Zhang Fei, Huang Xin, Liu Yu, Ding Lu, Xu Lin, Zhu Mao-Bi, Hu Wen-Feng, Qi Zhong-Quan, Wang Hai-Long, Yang Xiang-Jun
Department of Gynaecology and Obstetrics, Zhongshan Hospital, Xiamen University, Xiamen, Fujian Province, 361004, China.
Center of Reproductive Medicine, Women and Children Health Care Hospital of Xiamen, Xiamen, Fujian Province, 361003, China.
Reprod Fertil Dev. 2014 Oct;26(8):1084-93. doi: 10.1071/RD12332.
Meiosis produces haploid gametes for sexual reproduction. Triphenyltin chloride (TPTCL) is a highly bioaccumulated and toxic environmental oestrogen; however, its effect on oocyte meiosis remains unknown. We examined the effect of TPTCL on mouse oocyte meiotic maturation in vitro and in vivo. In vitro, TPTCL inhibited germinal vesicle breakdown (GVBD) and first polar body extrusion (PBE) in a dose-dependent manner. The spindle microtubules completely disassembled and the chromosomes condensed after oocytes were exposed to 5 or 10μgmL(-1) TPTCL. γ-Tubulin protein was abnormally localised near chromosomes rather than on the spindle poles. In vivo, mice received TPTCL by oral gavage for 10 days. The general condition of the mice deteriorated and the ovary coefficient was reduced (P<0.05). The number of secondary and mature ovarian follicles was significantly reduced by 10mgkg(-1) TPTCL (P<0.05). GVBD decreased in a non-significant, dose-dependent manner (P>0.05). PBE was inhibited with 10mgkg(-1) TPTCL (P<0.05). The spindles of in vitro and in vivo metaphase II oocytes were disassembled with 10mgkg(-1) TPTCL. These results suggest that TPTCL seriously affects meiotic maturation by disturbing cell-cycle progression, disturbing the microtubule cytoskeleton and inhibiting follicle development in mouse oocytes.
减数分裂产生用于有性生殖的单倍体配子。三苯基氯化锡(TPTCL)是一种具有高度生物累积性和毒性的环境雌激素;然而,其对卵母细胞减数分裂的影响尚不清楚。我们研究了TPTCL在体外和体内对小鼠卵母细胞减数分裂成熟的影响。在体外,TPTCL以剂量依赖的方式抑制生发泡破裂(GVBD)和第一极体排出(PBE)。当卵母细胞暴露于5或10μg/mL TPTCL后,纺锤体微管完全解体,染色体浓缩。γ-微管蛋白异常定位于染色体附近而非纺锤体极上。在体内,小鼠经口灌胃给予TPTCL 10天。小鼠的一般状况恶化,卵巢系数降低(P<0.05)。10mg/kg TPTCL显著降低了次级和成熟卵巢卵泡的数量(P<0.05)。GVBD呈非显著性剂量依赖性降低(P>0.05)。10mg/kg TPTCL抑制了PBE(P<0.05)。10mg/kg TPTCL使体外和体内中期II卵母细胞的纺锤体解体。这些结果表明,TPTCL通过干扰细胞周期进程、扰乱微管细胞骨架和抑制小鼠卵母细胞的卵泡发育,严重影响减数分裂成熟。