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Oocyte maturation and expression pattern of follicular genes during in-vitro culture of vitrified mouse pre-antral follicles

机译:玻璃化小鼠腹前卵泡体外培养过程中卵母细胞成熟和卵泡基因表达模式

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Our aim was to evaluate the oocyte maturation rate and follicular genes expression pattern during in-vitro culture of vitrified mouse pre-antral follicles. Middle sized pre-antral follicles were isolated mechanically from the ovaries of pre-pubertal mice and distributed in vitrification and control groups. In the vitrification group, follicles were washed in equilibration and vitrification solutions and then were immersed in liquid nitrogen after loading on cryotop tips. After warming in descending concentrations of sucrose solutions, fresh and vitrified-warmed follicles were cultured for 13 days. Follicles survival rate and follicular genes expression were assessed during in vitro culture. Finally, at the end of the culture period oocytes maturation rate were compared in both groups. In the vitrification group, follicles survival rate was lower significantly comparing to the control group (P < 0.05), whereas oocytes maturation rate were similar. Although at the beginning of the culture period, expression of some genes such as Gdf9, Bmp15, Tgf beta 1 and BmprII were higher in the vitrification group (P < 0.05), during the rest of the culture period expression pattern of all follicular genes were similar in both groups. In conclusion, survival rate of cryotop vitrified pre-antral follicles reduced during culture period while oocytes maturation and follicular genes expression did not show any noticeable alteration. (C) 2015 Elsevier B.V. All rights reserved.
机译:我们的目的是评估玻璃化的小鼠前肛门卵泡体外培养过程中的卵母细胞成熟率和卵泡基因表达模式。机械地从青春期前小鼠的卵巢中分离出中等大小的肛门前卵泡,并将其分布在玻璃化和对照组中。在玻璃化组中,将卵泡在平衡和玻璃化溶液中洗涤,然后将其装载在冷冻顶上后浸入液氮中。在降低浓度的蔗糖溶液中温热后,将新鲜和玻璃化温热的卵泡培养13天。在体外培养期间评估卵泡存活率和卵泡基因表达。最后,在培养期结束时比较两组的卵母细胞成熟率。玻璃化组的卵泡存活率明显低于对照组(P <0.05),而卵母细胞的成熟率相似。尽管在培养期开始时,玻璃化组中某些基因如Gdf9,Bmp15,Tgf beta 1和BmprII的表达较高(P <0.05),在培养期的其余时间内,所有卵泡基因的表达模式均为两组相似。总之,在培养期间,冷冻切片玻璃化的前肛门前卵泡的存活率降低,而卵母细胞成熟和卵泡基因表达未显示任何明显的变化。 (C)2015 Elsevier B.V.保留所有权利。

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