Ramezani Mahdi, Salehnia Mojdeh, Jafarabadi Mina
Department of Anatomical Sciences, Medical Sciences Faculty, Tarbiat Modares University, Tehran, Iran.
Reproductive Health Research Center, Tehran University of Medical Sciences, Tehran, Iran.
J Obstet Gynaecol Res. 2018 Mar;44(3):474-487. doi: 10.1111/jog.13530. Epub 2018 Jan 5.
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.
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.
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.
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.
本研究评估玻璃化冷冻程序对人促排卵卵巢组织在复温及体外培养两周后的完整性、形态、卵泡发育及基因表达的影响。
将卵巢标本分为非玻璃化冷冻组和玻璃化冷冻组,培养两周。进行形态学分析和免疫组织化学检测。评估收集培养基中17-β雌二醇和抗苗勒管激素水平。采用实时逆转录聚合酶链反应分析基因表达。
两组人促排卵卵巢组织中bcl-2样蛋白4和B细胞淋巴瘤2的形态及免疫组织化学结果相似。体外培养前后两组正常卵泡百分比无显著差异。尽管与未培养组相比,培养组织中生长卵泡百分比增加,但两组培养组织中正常卵泡率均显著降低(P<0.05)。玻璃化冷冻组织与对照组相比基因表达无差异;然而,在体外培养期间,生长分化因子9和卵泡刺激素受体基因表达增加,生殖系α因子和kit配体基因表达降低(P<0.05)。在两个培养组中,17-β雌二醇水平升高(P<0.05),但抗苗勒管激素浓度无统计学改变。
这些结果表明,玻璃化冷冻/复温后人促排卵卵巢组织的完整性得到了良好保存;然而,体外培养条件需要改进。