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首页> 外文期刊>Iranian Journal of Reproductive Medicine >COMPARING THE VIABILITY AND IN VITRO MATURATION OF CUMULUS GERMINAL VESICLE BREAK DOWN (GVBD) OOCYTE COMPLEXES USING TWO VITRIFICATION TECHNIQUES IN MICE
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COMPARING THE VIABILITY AND IN VITRO MATURATION OF CUMULUS GERMINAL VESICLE BREAK DOWN (GVBD) OOCYTE COMPLEXES USING TWO VITRIFICATION TECHNIQUES IN MICE

机译:使用两种玻璃化技术比较小鼠生殖道囊泡分解(GVBD)卵母细胞复合物的活性和体外成熟

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Background: Vitrification is assumed to be a promising method to cryopreserve human oocytes but still needs optimizing.Objective: The aim of this study was to improve the single step and step-wise vitrification effects on maturing mouse GVBD oocytes by ethylene glycol (EG) in conventional straws.Materials and Methods: Oocytes with compact cumulus cells were cultured for 3hr in TCM199 supplemented with 10% fetal bovine serum (FBS) in 5% CO2 in air. GVBD oocytes were randomly allocated into three groups. (1) Control (non-vitrified group), (2) exposed to single-step vitrification (contained of EG 20%+0.5M sucrose), (3) exposed to step-wise vitrification (2%, 5%, 10%, 20%EG +0.5M sucrose). In vitrification groups,oocytes were thawed and underwent additional 21 hr maturation. Viability of oocytes and maturation to MII stage were analyzed using inverted microscope and additionally by staining of propidium iodide and Hoechst 33342.Results: All non-vitrified oocytes were viable after 24 hr; however, viability of vitrified samples in single-step group was significantly lower than that of the step-wise and controls Groups. Also, the maturation rate in the step-wise group was significantly higher (p0.05) compared to single-step.Conclusion: These results suggest that step-wise vitrification of GVBD oocytes as compared to single step vitrification was better in the rate of survival and in vitro maturation of oocytes.
机译:背景:玻璃化被认为是冷冻保存人卵母细胞的一种有前途的方法,但仍需要优化。目的:本研究的目的是通过乙二醇(EG)改善成熟的小鼠GVBD卵母细胞的单步和逐步玻璃化作用。材料和方法:将卵母细胞与致密卵丘细胞在补充有10%胎牛血清(FBS)的5%CO2空气中的TCM199中培养3小时。 GVBD卵母细胞随机分为三组。 (1)对照组(非玻璃化组),(2)暴露于单步玻璃化(包含EG 20%+ 0.5M蔗糖),(3)暴露于逐步玻璃化(2%,5%,10% ,20%EG + 0.5M蔗糖)。在玻璃化组中,将卵母细胞解冻并再进行21小时的成熟。用倒置显微镜分析卵母细胞的活力和成熟至MII期,并通过碘化丙啶和Hoechst 33342染色。结果:所有未玻璃化的卵母细胞在24小时后均能存活;然而,单步法玻璃化样品的存活率明显低于逐步法和对照组。此外,与单步法相比,分步法组的成熟率显着更高(p <0.05)。结论:这些结果表明,与单步法相比,GVBD卵母细胞的分步法玻璃化率更高。卵母细胞的存活和体外成熟。

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