Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Department of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.
Zygote. 2021 Dec;29(6):468-475. doi: 10.1017/S0967199421000174. Epub 2021 Apr 29.
In vitro activation of primordial follicles could serve as a safe method to preserve fertility in patients with cancer subjected to ovarian tissue cryopreservation during oncotherapy, however the culture medium for this purpose requires to be optimized. Granulosa cell conditioned medium (GCCM) has been recognized to enhance primordial follicle activation and the present study was conducted to understand whether addition of pyruvate, a combination of insulin, transferrin and selenium (ITS) or testosterone to GCCM could improve its efficiency in this regard. To this end, 1-day-old mouse ovaries were cultured in four different media including CON (control; containing GGCM only), PYR (containing GCCM plus pyruvate), ITS (containing GCCM plus ITS) or TES (containing GCCM plus testosterone) for 11 days. Furthermore, follicular dynamics and gene expression of factors involved in follicular development were assessed using histological examination and RT-PCR, respectively, on days 5 and 11 of culture. Pyruvate decreased follicular activation, but it enhanced the progression of follicles to the primary stage. Moreover, it upregulated Bmp15 and Cx37 (P < 0.05). In the ITS group, activation of follicles was not affected and total number of follicles was reduced by day 11 of culture. Additionally, ITS downregulated Pi3k, Gdf9, Bmp15 and Cx37 (P < 0.05). Although testosterone did not affect primordial follicle activation, it enhanced the development of follicles up to the preantral stage (P < 0.05). Furthermore, testosterone inhibited the expression of Pten but stimulated the expression of Gdf9 and Cx37 (P < 0.05). In conclusion, the present study revealed that inclusion of pyruvate and testosterone into GCCM could enhance the early development of follicles in cultured 1-day-old mouse ovaries.
体外激活原始卵泡可以作为一种安全的方法,用于在接受癌症治疗的患者中通过卵巢组织冷冻保存来保留生育能力,然而为此目的的培养基需要进行优化。颗粒细胞条件培养基 (GCCM) 已被证明可以增强原始卵泡的激活,本研究旨在了解添加丙酮酸、胰岛素、转铁蛋白和硒 (ITS) 或睾酮到 GCCM 中是否可以提高其在这方面的效率。为此,将 1 天大的小鼠卵巢在四种不同的培养基中培养 11 天,包括 CON(对照;仅含有 GCCM)、PYR(含有 GCCM 和丙酮酸)、ITS(含有 GCCM 和 ITS)或 TES(含有 GCCM 和睾酮)。此外,在培养的第 5 和 11 天,通过组织学检查和 RT-PCR 分别评估卵泡动力学和参与卵泡发育的因子的基因表达。丙酮酸降低了卵泡的激活,但促进了卵泡向初级阶段的进展。此外,它上调了 Bmp15 和 Cx37(P<0.05)。在 ITS 组中,卵泡的激活没有受到影响,并且在培养的第 11 天卵泡的总数减少。此外,ITS 下调了 Pi3k、Gdf9、Bmp15 和 Cx37(P<0.05)。尽管睾酮不会影响原始卵泡的激活,但它可以促进卵泡发育到小腔前阶段(P<0.05)。此外,睾酮抑制了 Pten 的表达,但刺激了 Gdf9 和 Cx37 的表达(P<0.05)。总之,本研究表明,将丙酮酸和睾酮纳入 GCCM 可以增强培养的 1 天大的小鼠卵巢中卵泡的早期发育。