Effect of endometrial cell-conditioned medium and platelet-rich plasma on the developmental competence of mouse preantral follicles: An in vitro study.

IF 1.8 Q3 OBSTETRICS & GYNECOLOGY
Neda Taghizabet, Soghra Bahmanpour, Nehleh Zarei-Fard, Gholamreza Mohseni, Fereshteh Aliakbari, Farzaneh Dehghani
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Abstract

Objective: The aim of this study was to evaluate the impacts of platelet-rich plasma (PRP) and conditioned medium (CM) derived from endometrial stromal cells on mouse preantral follicle culture in a two-dimensional system to produce competent mature oocytes for fertilization.

Methods: In total, 240 preantral follicles were isolated from female mouse ovarian tissue and divided into four groups. The preantral follicles were isolated three times for each group and then cultured, respectively, in the presence of alpha minimum essential medium (control), PRP, CM, and PRP+CM. The in vitro growth, in vitro maturation, and cleavage percentage of the preantral follicles were investigated. Immunocytochemistry (IHC) was also conducted to monitor the meiotic progression of the oocytes. Additionally, the mRNA expression levels of the two folliculogenesis-related genes (Gdf9 and Bmp15) and two apoptosis-related genes (Bcl2 and Bax) were investigated using real-time polymerase chain reaction.

Results: In the PRP, CM, and PRP+CM groups, the preantral follicle maturation (evaluated by identifying polar bodies) were greater than the control group. The cleavage rate in the CM, and PRP+CM groups were also greater than the control group. IHC analysis demonstrated that in each treatment group, meiotic spindle was normal. In the PRP+CM group, the gene expression levels of Bmp15, Gdf9, and Bcl2 were greater than in the other groups. The Bax gene was more strongly expressed in the PRP and control groups than in the other groups.

Conclusion: Overall, the present study suggests that the combination of CM and PRP can effectively increase the growth and cleavage rate of mouse preantral follicles in vitro.

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Abstract Image

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子宫内膜细胞条件培养基和富血小板血浆对小鼠腔前卵泡发育能力影响的体外研究。
目的:本研究的目的是评估富血小板血浆(PRP)和子宫内膜基质细胞条件培养基(CM)对小鼠腔前卵泡在二维系统中培养产生可受精的成熟卵母细胞的影响。方法:从雌性小鼠卵巢组织中分离卵泡240个,分为4组。每组分离3次腔前卵泡,分别在α -最低基本培养基(对照)、PRP、CM和PRP+CM中培养。研究了腔前卵泡的体外生长、体外成熟和卵裂率。免疫细胞化学(IHC)监测卵母细胞减数分裂的进展。实时聚合酶链反应检测两种卵泡发生相关基因(Gdf9和Bmp15)和两种凋亡相关基因(Bcl2和Bax)的mRNA表达水平。结果:PRP组、CM组和PRP+CM组的腔前卵泡成熟度(通过识别极体来评估)高于对照组。CM组和PRP+CM组的卵裂率均大于对照组。免疫组化分析显示各治疗组减数分裂纺锤体正常。PRP+CM组Bmp15、Gdf9、Bcl2基因表达水平高于其他组。Bax基因在PRP组和对照组中的表达强于其他组。结论:总体而言,本研究提示CM与PRP联合使用可有效提高小鼠体外腔前卵泡的生长和卵裂率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
3.30
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