首页> 外文期刊>The Journal of Reproduction and Development >In vitro maturation of immature rat oocytes under simple culture conditions and subsequent developmental ability
【24h】

In vitro maturation of immature rat oocytes under simple culture conditions and subsequent developmental ability

机译:在简单培养条件下未成熟大鼠卵母细胞的体外成熟及其随后的发育能力

获取原文
           

摘要

Rat oocytes can be produced artificially by superovulation. Because some strains show low sensitivity to superovulation treatment, in vitro maturation is an alternative method to produce numerous matured oocytes. Furthermore, establishment of an in vitro maturation system with simple culture conditions is cost effective and leads to easy handling of oocytes. This study examined developmental ability of rat germinal vesicle (GV) oocytes maturing in vitro under simple culture conditions. Significantly different numbers of ovulated oocytes reached the second metaphase of meiosis (MII) among Jcl:Wistar (17.0), F344/Stm (31.0), and BN/SsNSlc (2.2) rats in whom superovulation was induced by pregnant mare serum gonadotropin (PMSG) and human chorionic gonadotropin. However, similar numbers of GV oocytes were obtained from ovaries of PMSG-injected Wistar (27.7), F344 (34.7), and BN (24.7) rats. These GV oocytes were cultured in vitro in HTF, αMEM, and a 1:1 HTF + αMEM or TYH + αMEM mixture. High proportions of Wistar and F344 oocytes that matured to MII in αMEM were parthenogenetically activated by strontium chloride treatment (78% and 74%, respectively). Additionally, 10% of matured oocytes of both strains developed into offspring after intracytoplasmic sperm injection and embryo transfer to foster mothers. Although BN oocytes cultured in αMEM could be parthenogenetically activated and developed into offspring, the success rate was lower than that for Wistar and F344 oocytes. This study demonstrated that numerous GV oocytes were produced in rat ovaries by PMSG injection. This simple in vitro maturation system of immature oocytes could be further developed to maintain valuable rat strains experiencing reproductive difficulties.
机译:大鼠卵母细胞可以通过超排卵人工产生。由于某些菌株对超排卵治疗的敏感性较低,因此体外成熟是产生大量成熟卵母细胞的另一种方法。此外,建立具有简单培养条件的体外成熟系统具有成本效益,并且易于处理卵母细胞。这项研究审查了在简单的培养条件下体外成熟的大鼠发芽囊泡(GV)卵母细胞的发育能力。在Jcl:Wistar(17.0),F344 / Stm(31.0)和BN / SsNSlc(2.2)大鼠中,通过怀孕母马血清促性腺激素(PMSG)诱导超排卵的排卵卵母细胞进入减数分裂第二中期的数量明显不同。 )和人类绒毛膜促性腺激素。但是,从注射PMSG的Wistar(27.7),F344(34.7)和BN(24.7)大鼠的卵巢中获得了相似数量的GV卵母细胞。这些GV卵母细胞在HTF,αMEM和1:1 HTF +αMEM或TYH +αMEM混合物中进行体外培养。在αMEM中成熟成MII的高比例Wistar和F344卵母细胞通过氯化锶处理被孤雌性激活(分别为78%和74%)。此外,两种品系的成熟卵母细胞中有10%的卵母细胞内注射精子并通过胚胎移植来培养后代后代。尽管在αMEM中培养的BN卵母细胞可以被孤雌性激活并发展为后代,但成功率低于Wistar和F344卵母细胞。这项研究表明,通过PMSG注射在大鼠卵巢中产生了大量GV卵母细胞。可以进一步开发这种简单的未成熟卵母细胞体外成熟系统,以维持有价值的大鼠品系经历繁殖困难。

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