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首页> 外文期刊>Asian journal of animal and veterinary advances >Comparison of Mouse Embryo Cleavage Rate from One Cell Stage to Blastocyst Stage in Co-culture with Vero Cells and Without Co-culture
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Comparison of Mouse Embryo Cleavage Rate from One Cell Stage to Blastocyst Stage in Co-culture with Vero Cells and Without Co-culture

机译:在有Vero细胞和没有共培养的情况下,共培养的小鼠胚胎从一个细胞阶段到囊胚阶段的裂解率比较

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The aim of this study was to evaluate the effects of Vero cells on early embryonic cleavage rate and overcome cellblock of mice embryos in vitro . Female mice were super-ovulated by Intra-peritoneal injection of 5 IU Pregnant mare serum gonadotropine (PMSG) and 5 IU Human Chorionic Gonadotropine (HCG) 48 h later. The super-ovulated female NMRI mice placed individually with NMRI (Noda Medical Research Institute) males of proved fertility. The following morning, the females with positive vaginal plug were killed and cumulus-enclosed single cell embryos (2PN) were recovered. Two pronuclear (n=170) embryos were divided randomly into 2 groups: (1) co culture with vero cells (2) culture in simple culture medium. The rate of the development and the morphological appearance of mouse embryos in two groups were recorded daily for 120 h after retrieval in each system using inverted microscope. On day 5 of development the results showed that embryos cultured on vero cells had a significantly higher blastocyst and hatching formation rate than those in simple culture medium alone (p<0.05). It is concluded that Vero cells may improve mouse embryo development partly by increasing blastocyst formation, hatching blastocyst rate.
机译:本研究的目的是评估Vero细胞对小鼠早期胚胎卵裂率的影响,并克服小鼠胚胎的细胞阻滞作用。 48小时后,通过腹膜内注射5 IU怀孕母马血清促性腺激素(PMSG)和5 IU人绒毛膜促性腺激素(HCG)对雌性小鼠进行超排卵。将超排卵的NMRI雌性小鼠与经证实具有生育能力的NMRI(Noda医学研究所)雄性单独放置。第二天早晨,杀死具有阳性阴道栓的雌性,并回收了积聚卵的单细胞胚胎(2PN)。将两个原核(n = 170)胚胎随机分为2组:(1)与vero细胞共培养(2)在简单培养基中培养。使用倒置显微镜在每个系统中检索120小时后,每天记录两组小鼠胚胎的发育速率和形态外观。在发育的第5天,结果显示,在vero细胞上培养的胚胎的胚泡和孵化率比单独在简单培养基中的胚泡和孵化率要高得多(p <0.05)。结论是,Vero细胞可部分通过增加胚泡形成,孵化胚泡率来改善小鼠胚胎的发育。

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