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首页> 外文期刊>The journal of obstetrics and gynaecology research >Vitrification and in vitro in vitro culture had no adverse effect on the follicular development and gene expression of stimulated human ovarian tissue
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Vitrification and in vitro in vitro culture had no adverse effect on the follicular development and gene expression of stimulated human ovarian tissue

机译:玻璃化和体外体外培养对刺激的人卵巢组织的卵泡发育和基因表达没有不利影响

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Abstract Aim The study assesses the effect of the vitrification procedure on the integrity, morphology, follicular development and gene expression of stimulated human ovarian tissue after warming and two weeks of in vitro culture. Methods Ovarian specimens were divided into non‐vitrified and vitrified groups and were cultured for two weeks. Morphological analysis and immunohistochemistry were performed. The 17‐β estradiol and anti‐Müllerian hormone levels in collected media were assessed. Gene expression was analyzed using real‐time reverse transcription polymerase chain reaction. Results The morphology and immunohistochemistry of bcl‐2‐like protein 4 and B‐cell lymphoma 2 of human stimulated ovarian tissue were similar in both groups. There was no significant difference in the percentage of normal follicles between the groups before and after in vitro culture. In spite of an increase in the percentage of growing follicles in cultured tissues compared to the non‐cultured groups, the rate of normal follicles was significantly decreased in both cultured groups ( P 0.05). Gene expression was no different in vitrified tissues compared to the control; however, the expression of growth differentiation factor 9 and follicle stimulating hormone receptor genes were increased and factor in germ line alpha and kit ligand genes were decreased during in vitro culture ( P 0.05). In the two cultured groups, the level of 17‐β estradiol was increased ( P 0.05), but the anti‐Müllerian hormone concentration was not statistically altered. Conclusions These results showed that the integrity of stimulated human ovarian tissue after vitrification/warming was well preserved; however, the in vitro culture condition needs improvement.
机译:摘要目的该研究评估玻璃化程序对刺激的人卵巢组织在变暖后的完整性,形态,卵泡发育和基因表达的影响,以及两周的体外培养。方法将卵巢标本分为非玻璃化和玻璃化基团,并培养两周。进行形态分析和免疫组织化学。评估收集培养基中的17-β雌二醇和抗Müllerian热量水平。使用实时逆转录聚合酶链反应分析基因表达。结果两组中,人刺激卵巢组织Bcl-2样蛋白4和B细胞淋巴瘤2的形态和免疫组织化学相似。在体外培养之前和之后,组之间的正常卵泡百分比没有显着差异。尽管与非培养基团的培养组织中生长卵泡的百分比增加,但培养基团中正常卵泡的速率显着降低(P <0.05)。与对照相比,基因表达在玻璃化组织中没有任何不同;然而,增加生长分化因子9和卵泡刺激激素受体基因的表达,并且在体外培养期间(P <0.05)期间胚芽线α和试剂盒配体基因的因子降低。在两组中,17-β雌二醇的水平增加(P <0.05),但抗Müllerian激素浓度没有统计变化。结论这些结果表明,玻璃化/升温后刺激的人卵巢组织的完整性得到了保存良好;然而,体外培养条件需要改善。

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