A dual-drug strategy to enhance the function of cryopreserved ovaries by promoting revascularization and inhibiting follicle over-activation.

IF 4.7 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Lingyu Li, Jian Yang, Longzhong Jia, Jing Liang, Kaixin Cheng, Xuebing Yang, Lu Mu, Ge Wang, Kaiying Geng, Qiuxian Hu, Xueqiang Xu, Zhen Li, Guoliang Xia, Ting Guo, Jiawei Zhang, Yan Zhang, Hua Zhang
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引用次数: 0

Abstract

Background: Ovarian tissue cryopreservation and transplantation (OTCT) is a promising approach for fertility preservation. However, significant follicle loss after transplantation challenges long-term reproductive recovery. Although primordial follicle loss and ischemic damage are known contributors, the underlying mechanisms and effective strategies to mitigate these damages are still lacking.

Methods: Ovarian tissues from wild-type or Tek-CreERT2;mTmG female mice were cryopreserved using vitrification. Follicle dynamics after OTCT were analyzed through histology, proteomics, and high-resolution imaging. To assess protective effects, cryopreserved ovaries were treated with 500 nM rapamycin (Rapa), an inhibitor of primordial follicle activation; 5 ng/mL vascular endothelial growth factor A (VEGFA), which promotes angiogenesis; or both (Cryo + VRCS, VEGFA-Rapa Combination Strategy). DMSO or H2O served as controls. Grafts were collected at 3, 7, 14, and 120 days post-transplantation, with measurements of vascular density, tip cell density, follicle activation, and remaining follicles. Oocyte quality was evaluated via in vitro fertilization, and graft lifespan was estimated through estrous cycle monitoring.

Results: Our study observed a rapid decline in follicle numbers shortly after transplantation in a mouse model. Proteomic analysis and high-resolution 3D imaging revealed that this depletion was primarily due to damage to tip cells, which are crucial for angiogenesis, and the overactivation of dormant primordial follicles. Damage to tip cells compromised vascular reconstruction, leading to ischemic injury, while mechanical handling during tissue isolation and cryopreservation triggered excessive follicle activation. We implemented a combination therapy using rapamycin to inhibit follicle activation and VEGFA to promote angiogenesis prior to transplantation. This approach significantly improved follicle survival, extended reproductive function, and enhanced oocyte quality.

Conclusion: Our study provides a practical strategy for preserving the reproductive potential of cryopreserved ovarian tissues by simultaneously targeting vascular integrity and follicle stability through the dual drug strategy of VEGFA and rapamycin combine treatment.

通过促进血管重建和抑制卵泡过度激活来增强冷冻卵巢功能的双重药物策略。
背景:卵巢组织冷冻保存和移植(OTCT)是一种很有前途的生育保存方法。然而,移植后显著的卵泡损失对长期生殖恢复构成挑战。虽然原始卵泡损失和缺血性损伤是已知的贡献者,但仍然缺乏潜在的机制和有效的策略来减轻这些损害。方法:采用玻璃化冷冻保存野生型或Tek-CreERT2;mTmG雌性小鼠卵巢组织。通过组织学、蛋白质组学和高分辨率成像分析OTCT后卵泡动力学。为了评估保护作用,将冷冻保存的卵巢用500 nM雷帕霉素(Rapa)处理,雷帕霉素是一种原始卵泡激活抑制剂;5 ng/mL血管内皮生长因子A (VEGFA),促进血管生成;或两者兼而有之(Cryo + VRCS, VEGFA-Rapa组合策略)。DMSO或H2O作为对照。在移植后3、7、14和120天采集移植物,测量血管密度、尖端细胞密度、卵泡激活和剩余卵泡。通过体外受精评估卵母细胞质量,通过情周期监测评估移植物寿命。结果:我们的研究在小鼠模型中观察到移植后不久卵泡数量迅速下降。蛋白质组学分析和高分辨率3D成像显示,这种消耗主要是由于尖端细胞的损伤和休眠的原始卵泡的过度激活,尖端细胞对血管生成至关重要。尖端细胞损伤损害血管重建,导致缺血性损伤,而组织分离和低温保存期间的机械处理会引发过度的卵泡激活。我们在移植前使用雷帕霉素抑制卵泡激活和VEGFA促进血管生成的联合治疗。这种方法显著提高了卵泡存活率,延长了生殖功能,提高了卵母细胞质量。结论:我们的研究提供了一种实用的策略,通过VEGFA和雷帕霉素联合治疗,同时针对血管完整性和卵泡稳定性,保护冷冻卵巢组织的生殖潜力。
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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来源期刊
Reproductive Biology and Endocrinology
Reproductive Biology and Endocrinology 医学-内分泌学与代谢
CiteScore
7.90
自引率
2.30%
发文量
161
审稿时长
4-8 weeks
期刊介绍: Reproductive Biology and Endocrinology publishes and disseminates high-quality results from excellent research in the reproductive sciences. The journal publishes on topics covering gametogenesis, fertilization, early embryonic development, embryo-uterus interaction, reproductive development, pregnancy, uterine biology, endocrinology of reproduction, control of reproduction, reproductive immunology, neuroendocrinology, and veterinary and human reproductive medicine, including all vertebrate species.
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