首页> 外文期刊>Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society >The effect of leukemia inhibitory factor and coculture on the in vitro maturation and ultrastructure of vitrified and nonvitrified isolated mouse preantral follicles.
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The effect of leukemia inhibitory factor and coculture on the in vitro maturation and ultrastructure of vitrified and nonvitrified isolated mouse preantral follicles.

机译:白血病抑制因子和共培养对玻璃化和非玻璃化离体小鼠腔前卵泡体外成熟和超微结构的影响。

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OBJECTIVE: To develop a system for in vitro maturation of preantral follicles isolated from vitrified and nonvitrified mouse ovaries by leukemia inhibitory factor (LIF) and coculture with cumulus cells. DESIGN: Experimental study. SETTING: University-based research laboratory. ANIMAL(S): Twelve- to 14-day-old National Medical Research Institute female mice. INTERVENTION(S): Vitrification of mouse ovaries and in vitro maturation of follicles. MAIN OUTCOME MEASURE(S): The growth, maturation, steroidogenesis, alkaline phosphatase activity, and ultrastructure of preantral follicles derived from vitrified and nonvitrified mouse ovaries and the developmental capacity of embryos obtained from metaphase II to blastocyst stage. RESULT(S): The follicular diameters were increased in the presence of LIF in the simple culture, coculture, and vitrified coculture groups. The survival and developmental rates of follicles were not significantly different between groups. The E(2) production was increased in all groups during the culture period. Alkaline phosphatase activity was observed in the follicles of cryosectioned slices and cultured preantral follicles. There was no remarkable change in ultrastructural maturation features of cultured follicles. CONCLUSION(S): LIF alone or in combination with the coculture system increased the growth of cultured preantral follicles but had no effect on their maturation; the ultrastructure, growth, and maturation of vitrified follicles were the same in the cultured groups and in the controls.
机译:目的:开发一种通过白血病抑制因子(LIF)从玻璃化和未玻璃化的小鼠卵巢分离的前壁卵泡的体外成熟系统,并与卵丘细胞共培养。设计:实验研究。地点:大学研究实验室。动物:12至14天大的国家医学研究所雌性小鼠。干预:小鼠卵巢玻璃化和卵泡体外成熟。主要观察指标:玻璃化和非玻璃化小鼠卵巢的前壁卵泡的生长,成熟,类固醇生成,碱性磷酸酶活性和超微结构,以及从中期II到胚泡期的胚胎的发育能力。结果:在简单培养,共培养和玻璃化共培养组中,存在LIF时卵泡直径增加。各组之间卵泡的存活率和发育率无显着差异。在培养期间,所有组的E(2)产量均增加。在冷冻切片的卵泡和培养的窦前卵泡中观察到碱性磷酸酶活性。培养的卵泡的超微结构成熟特征没有显着变化。结论:单独或与共培养系统联合使用的LIF促进了培养的腔前卵泡的生长,但对它们的成熟没有影响。玻璃化卵泡的超微结构,生长和成熟在培养组和对照组中是相同的。

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