Alborzi Parimah, Jafari Atrabi Mohammad, Akbarinejad Vahid, Khanbabaei Ramezan, Fathi Rouhollah
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. 2020 Jun 2:1-8. doi: 10.1017/S096719942000026X.
In vitro activation of primordial follicles provides cancer patients subjected to oncotherapy with a safe therapeutic strategy for fertility preservation, however a successful protocol for activation of primordial follicles in prepubertal patients has not yet been defined comprehensively. There is evidence that amino acids such as leucine, arginine and glutamine could stimulate the mammalian target of rapamycin (mTOR) pathway, which plays a pivotal role in primordial follicle activation. Nevertheless, there has been no report that elucidates the effect of these amino acids on in vitro development of ovarian follicles. Therefore, the present study was conducted to evaluate the effects of these amino acids and their combination on the formation and activation of primordial follicles in 1-day-old murine ovaries during an 11-day culture period. The experimental groups consisted of base medium (BM), base medium + arginine (ARG), base medium + glutamine (GLU), base medium + leucine (LEU) and base medium + a combination of arginine, glutamine and leucine (AGL). The proportions of different stages of ovarian follicles and gene expression of regulatory factors were assessed using histology and quantitative real-time PCR on days 5 and 11 of culture. The proportion of transitional and primary follicles was greater in all amino acid-treated groups compared with the BM group (P < 0.05). Moreover, leucine resulted in elevated expression of Gdf9 and Bmp15, and glutamine augmented the expression of Pi3k on day 11 of culture. In conclusion, the present study showed that inclusion of leucine, glutamine, arginine or their combination in the culture medium for murine ovarian tissue could accelerate the activation of primordial follicles and alter the expression of the corresponding factors.
原始卵泡的体外激活为接受肿瘤治疗的癌症患者提供了一种安全的生育力保存治疗策略,然而,尚未全面确定一种成功的青春期前患者原始卵泡激活方案。有证据表明,亮氨酸、精氨酸和谷氨酰胺等氨基酸可以刺激雷帕霉素哺乳动物靶标(mTOR)通路,该通路在原始卵泡激活中起关键作用。然而,尚无报道阐明这些氨基酸对卵巢卵泡体外发育的影响。因此,本研究旨在评估这些氨基酸及其组合在11天培养期内对1日龄小鼠卵巢中原始卵泡形成和激活的影响。实验组包括基础培养基(BM)、基础培养基+精氨酸(ARG)、基础培养基+谷氨酰胺(GLU)、基础培养基+亮氨酸(LEU)和基础培养基+精氨酸、谷氨酰胺和亮氨酸组合(AGL)。在培养的第5天和第11天,使用组织学和定量实时PCR评估卵巢卵泡不同阶段的比例和调节因子的基因表达。与BM组相比,所有氨基酸处理组的过渡卵泡和初级卵泡比例均更高(P<0.05)。此外,亮氨酸导致培养第11天Gdf9和Bmp15表达升高,谷氨酰胺增强了Pi3k的表达。总之,本研究表明,在小鼠卵巢组织培养基中添加亮氨酸、谷氨酰胺、精氨酸或其组合可加速原始卵泡的激活并改变相应因子的表达。