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首页> 外文期刊>Stem Cell Research & Therapy >Small extracellular vesicles derived from embryonic stem cells restore ovarian function of premature ovarian failure through PI3K/AKT signaling pathway
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Small extracellular vesicles derived from embryonic stem cells restore ovarian function of premature ovarian failure through PI3K/AKT signaling pathway

机译:通过PI3K / AKT信号通路恢复胚胎干细胞的小细胞外囊泡恢复过早卵巢衰竭的卵巢功能

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BACKGROUND:Premature ovarian failure (POF) has a great impact on reproductive endocrine function in females, and it is an important cause of infertility. Previous studies have demonstrated that small extracellular vesicles (sEVs) derived from stem cells play an important role in tissue regeneration. This study aimed to investigate the therapeutic effect of sEVs derived from embryonic stem cells (ESCs-sEVs) on damaged ovaries and explore the underlying molecular mechanisms.METHODS:Mice POF models were established by injecting mice with cyclophosphamide and busulfan. Then, ESCs-sEVs were intravenously transplanted into POF mice. The plasma of mice was harvested at 1 and 2?weeks after treatment to analyze the levels of anti-Mullerian hormone (AMH), estradiol (Esub2/sub), and follicle stimulating hormone (FSH) by ELISA. The morphology of ovaries and follicles was observed by H&E staining, and apoptosis of granulosa cells was detected by TUNEL. In vitro, EdU and CCK-8 tests were used to evaluate the proliferation of cultured granulosa cells stimulated by ESCs-sEVs. Western blotting was used to determine the expression of PI3K/AKT and apoptotic-related proteins.RESULTS:After transplantation of ESCs-sEVs, the levels of serum sex hormones recovered to normal levels. In addition, the number of follicles was significantly increased, and the number of apoptotic cells was decreased. The results in vitro revealed that ESCs-sEVs could significantly improve the proliferation rate of granulosa cells and increase the expression of phosphorylated PI3K and AKT. Meanwhile, the positive effect on proliferation and the negative effect on apoptosis observed in granulosa cells were obviously decreased when the PI3K/AKT signaling pathway was inhibited.CONCLUSION:Our findings suggested that ESCs-sEVs could improve ovarian function by regulating the PI3K/AKT signaling pathway, which could provide a promising clinical therapy for POF.
机译:背景:早产卵巢衰竭(POF)对女性的生殖内分泌功能有很大影响,这是不孕症的重要原因。以前的研究表明,衍生自干细胞的小细胞外囊泡(SEVS)在组织再生中发挥着重要作用。本研究旨在探讨衍生自胚胎干细胞(ESCS-SEV)对损伤卵巢(ESCS-SEV)的治疗效果,探讨潜在的分子机制。方法:通过环磷酰胺和鸟类注射小鼠建立小鼠POF模型。然后,将Escs-eD静脉内移植到POF小鼠中。在治疗后1和2周收获小鼠的血浆,分析抗Mullerian激素(AMH),雌二醇(E 2 )的水平,并通过ELISA刺激激素(FSH)。 H&E染色观察卵巢和卵泡的形态,并通过TUNEL检测颗粒细胞细胞凋亡。体外,EDU和CCK-8试验用于评估由ESC-SED刺激的培养的颗粒细胞的增殖。用于确定PI3K / AKT和凋亡相关蛋白的表达。结果:在移植ESC-SED后,恢复到正常水平的血清性激素水平。此外,卵泡的数量显着增加,凋亡细胞的数量降低。体外结果表明,ESC-SED可以显着提高颗粒细胞的增殖速率,并增加磷酸化PI3K和Akt的表达。同时,当抑制PI3K / AKT信号通路时明显减少了对颗粒细胞中观察到的对细胞凋亡的积极影响。结论:我们的研究结果表明ESC-SED可以通过调节PI3K / AKT信号来改善卵巢功能途径可以为POF提供有希望的临床疗法。

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