MSCs-derived EVs protect against chemotherapy-induced ovarian toxicity: role of PI3K/AKT/mTOR axis.

IF 3.8 3区 医学 Q1 REPRODUCTIVE BIOLOGY
Nehal M Elsherbiny, Mohamed S Abdel-Maksoud, Kousalya Prabahar, Zuhair M Mohammedsaleh, Omnia A M Badr, Arigue A Dessouky, Hoda A Salem, Omnia A Refadah, Ayman Samir Farid, Ashraf A Shamaa, Nesrine Ebrahim
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引用次数: 0

Abstract

Chemotherapy detrimentally impacts fertility via depletion of follicular reserves in the ovaries leading to ovarian failure (OF) and development of estrogen deficiency-related complications. The currently proposed options to preserve fertility such as Oocyte or ovarian cortex cryopreservation are faced with many technical obstacles that limit their effective implementation. Therefore, developing new modalities to protect ovarian function remains a pending target. Exosomes are nano-sized cell-derived extracellular vesicles (EVs) with documented efficacy in the field of regenerative medicine. The current study sought to determine the potential beneficial effects of mesenchymal stem cells (MSCs)-derived EVs in experimentally induced OF. Female albino rats were randomly allocated to four groups: control, OF group, OF + MSCs-EVs group, OF + Rapamycin (mTOR inhibitor) group, and OF + Quercetin (PI3K/AKT inhibitor) group. Follicular development was assessed via histopathological and immunohistochemical examination, and ovarian function was evaluated by hormonal assay. PI3K/Akt/mTOR signaling pathway as a key modulator of ovarian follicular activation was also assessed. MSCs-EVs administration to OF rats resulted in restored serum hormonal levels, preserved primordial follicles and oocytes, suppressed ovarian PI3K/AKT axis and downstream effectors (mTOR and FOXO3), modulated miRNA that target this axis, decreased expression of ovarian apoptotic markers (BAX, BCl2) and increased expression of proliferation marker Ki67. The present study validated the effectiveness of MSCs-EVs therapy in preventing ovarian insufficiency induced by chemotherapy. Concomitant MSCs-EVs treatment during chemotherapy could significantly preserve ovarian function and fertility by suppressing the PI3K/Akt axis, preventing follicular overactivation, maintaining normal ovarian cellular proliferation, and inhibiting granulosa cell apoptosis.

间充质干细胞衍生的EV可防止化疗引起的卵巢毒性:PI3K/AKT/mTOR轴的作用
化疗会消耗卵巢中的卵泡储备,导致卵巢功能衰竭(OF)和雌激素缺乏相关并发症的发生,从而对生育能力产生不利影响。目前提出的卵母细胞或卵巢皮质冷冻保存等保留生育能力的方案面临许多技术障碍,限制了其有效实施。因此,开发保护卵巢功能的新方法仍是一个有待实现的目标。外泌体(Exosomes)是一种纳米级细胞衍生胞外囊泡(EVs),在再生医学领域具有有据可查的疗效。本研究旨在确定间充质干细胞(MSCs)衍生的EVs对实验性OF的潜在有益作用。雌性白化大鼠被随机分为四组:对照组、OF 组、OF + 间充质干细胞-EVs 组、OF + 雷帕霉素(mTOR 抑制剂)组和 OF + 槲皮素(PI3K/AKT 抑制剂)组。卵泡发育情况通过组织病理学和免疫组化检查进行评估,卵巢功能通过激素测定进行评估。此外,还评估了作为卵巢卵泡激活关键调节因子的PI3K/Akt/mTOR信号通路。给OF大鼠服用间充质干细胞-EVs后,血清激素水平得到恢复,原始卵泡和卵母细胞得以保留,卵巢PI3K/AKT轴及其下游效应因子(mTOR和FOXO3)受到抑制,靶向该轴的miRNA受到调节,卵巢凋亡标志物(BAX和BCl2)的表达减少,增殖标志物Ki67的表达增加。本研究验证了间充质干细胞-EVs疗法在预防化疗引起的卵巢功能不全方面的有效性。通过抑制PI3K/Akt轴,防止卵泡过度活化,维持卵巢细胞正常增殖,抑制颗粒细胞凋亡,化疗期间同时使用间充质干细胞-EVs治疗可显著保护卵巢功能和生育能力。
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来源期刊
Journal of Ovarian Research
Journal of Ovarian Research REPRODUCTIVE BIOLOGY-
CiteScore
6.20
自引率
2.50%
发文量
125
审稿时长
>12 weeks
期刊介绍: Journal of Ovarian Research is an open access, peer reviewed, online journal that aims to provide a forum for high-quality basic and clinical research on ovarian function, abnormalities, and cancer. The journal focuses on research that provides new insights into ovarian functions as well as prevention and treatment of diseases afflicting the organ. Topical areas include, but are not restricted to: Ovary development, hormone secretion and regulation Follicle growth and ovulation Infertility and Polycystic ovarian syndrome Regulation of pituitary and other biological functions by ovarian hormones Ovarian cancer, its prevention, diagnosis and treatment Drug development and screening Role of stem cells in ovary development and function.
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