首页> 外文期刊>Cryobiology: International Journal of Low Temperature Biology and Medicine >Effect of vitrification of in vitro matured prepubertal goat oocytes on embryo development after parthenogenic activation and intracytoplasmic sperm injection
【24h】

Effect of vitrification of in vitro matured prepubertal goat oocytes on embryo development after parthenogenic activation and intracytoplasmic sperm injection

机译:体外成熟的预先用山羊卵母细胞玻璃化对营养活化和血管科学性精子后胚胎发育的影响

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

This work studies the effect of vitrification of in vitro matured (IVM) prepubertal goat oocytes on: 1) oocyte damage assessed by reactive oxygen species (ROS) level and apoptosis and 2) embryo development after Intracytoplasmic sperm injection (ICSI) and Parthenogenic Activation (PA). Oocytes were IVM in supplemented TCM-199 for 22-24 h. Control group oocytes matured during 24 h were directly used for the analysis after IVM. Vitrified/warmed IVM-oocytes were vitrified after 22 h of IVM in 15% ethylene glycol (EG), 15% dimethyl sulfoxide (Me2SO) and 0.5 M sucrose and after subjected to warming procedure. Oocyte ROS level was measured by staining denuded IVM-oocytes with 10 mu M 2'7' dichlorodihydrofluorescein diacetate. Apoptosis was analyzed by Annexin V (AV) Apoptosis Detection kit and Propidium iodide (PI) signal and oocytes were classified as: Live (AV(-) PI-), early apoptotic (AV(+) PI-), dead non-apoptotic (AV(-) PI+) and necrotic (AV(+) PI+). Developmental competence of vitrified/warmed oocytes was assessed by PA (5 min in 5 mu M Ionomycin plus 4 h in 2 mM 6-Dimethylaminopurine), and by ICSI fertilization. Presumptive zygotes were in vitro cultured for 8 days in commercial media BO-IVC. Vitrified/warmed oocytes showed higher ROS levels (P < 0.0001), lower live oocytes (44 vs. 66%; P: 0.0025) and higher dead non-apoptotic oocytes (33 vs. 13% P: 0.023) compared to control. No differences were found on normal zygote formation (2 PN) (32 vs. 25%) or blastocyst development (0 vs. 4%) after ICSI fertilization. However, after PA, significant differences were found in cleavage rate (59 vs. 78%; P < 0.0343) and blastocyst formation (1 vs. 25%; P < 0.0001). In conclusion, vitrification reduced oocyte competence by increasing dead oocytes and ROS levels.
机译:这项工作研究了体外成熟(IVM)Prepubertal山羊卵母细胞的玻璃化效果:1)反应性氧物种(ROS)水平和凋亡评估的卵母细胞损伤和2)胚胎产生后的胚胎发育(ICSI)和营养活化后( PA)。卵母细胞在补充TCM-199中的IVM为22-24小时。对照组在24小时内成熟的卵母细胞直接用于IVM后的分析。在15%乙二醇(例如),15%二甲基亚砜(ME2SO)和0.5μm蔗糖中和进行加温过程后,玻璃化/升温的IVM-OVM-oOcytes在22小时后玻璃化。通过染色剥落的IVM-oOcytes测量卵母线ROS水平,其中10μm2'7'2'7'Dishlodihydrofluordclecleceine酸钠。通过膜蛋白v(AV)凋亡检测试剂盒和碘化丙烯酸铅(PI)信号和卵母细胞分析细胞凋亡分析为:活(AV( - )PI-),早期凋亡(AV(+)pi-),死亡的非凋亡(AV( - )PI +)和坏死(AV(+)PI +)。通过Pa(50mM M离子霉素在2mM 6-二甲基氨基嘧啶中5分钟,5分钟,通过ICSI施肥来评估玻璃化/温卵母细胞的发育能力。推定的Zygotes在商业媒体Bo-IVC中培养8天。玻璃化/升温卵母细胞显示出较高的ROS水平(P <0.0001),降低活卵母细胞(44 vs.66%; P:0.0025)和更高的死亡非凋亡卵母细胞(33 Vs.13%P:0.023)与对照相比。在ICSI施肥后,在正常的自由克氏料形成(2 pn)(2 pn)(2 pn)(32 vs.25%)或胚泡发育(0 vs.4%)上没有发现差异。然而,在PA之后,在切割率(59 vs.78%; P <0.0343)和胚泡形成(1 vs.25%; P <0.0001)中,发现显着差异。总之,玻璃化通过增加死亡卵母细胞和ROS水平来降低卵母细胞能力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号