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预处理细胞外囊泡作为一种纳米治疗策略,用于增强卵巢早衰和激素下降模型中颗粒细胞的功能。

Primed Extracellular Vesicles as a Nanotherapeutic Strategy to Enhance Granulosa Cell Function in a Model of Premature Ovarian Insufficiency and Hormonal Decline.

作者信息

Shieh Ju-Sheng, Chin Yu-Tang, Guo Jiong Jiong, Chiu Hsien-Chung, Cheng Hui-Rong, Hsu Hung-Han, Huang Chuang-Yen, Chen Yu-Hsuan, Hsieh Ya-Yu, Chang Fung-Wei

机构信息

Department of Periodontology, School of Dentistry, Tri-Service General Hospital and National Defense Medical University, Taipei City, Taiwan.

Department of Obstetrics and Gynecology, Tri-Service General Hospital and National Defense Medical University, Taipei City, Taiwan.

出版信息

Int J Nanomedicine. 2025 Sep 11;20:11099-11117. doi: 10.2147/IJN.S533393. eCollection 2025.

Abstract

BACKGROUND

Premature ovarian insufficiency (POI) is characterized by granulosa cell (GC) dysfunction, reduced steroidogenesis, and hypoestrogenism, often secondary to chemotherapy. Despite advancements in regenerative medicine, cell-free nanotherapies remain underexplored for POI treatment.

PURPOSE

This study investigates the therapeutic efficacy of primed avian mesenchymal stem cell-derived small extracellular vesicles (primed AMSC-sEVs) in a cyclophosphamide (CTX)-induced GC injury model, mimicking POI-associated hormonal dysfunction.

METHODS

Primed AMSC-sEVs were characterized in terms of particle size, concentration, and zeta potential using the Exoid TRPS and electrophoretic mobility platforms. Functional comparisons between primed and naïve AMSC-sEVs were conducted in human granulosa cells (hGCs), evaluating cell viability, apoptosis, steroidogenesis, and ovarian function-associated gene expression. miRNA content was assessed by next-generation sequencing and qRT-PCR.

RESULTS

Primed AMSC-sEVs displayed a smaller, more uniform size distribution, significantly enhanced particle concentration, and greater negative zeta potential (mean -24.4 mV vs -13.3 mV), suggesting improved colloidal stability. In vitro, primed sEVs dose-dependently enhanced hGC proliferation, restored CTX-induced suppression of AMH, FSHR, and LHCGR, and elevated estradiol and progesterone levels. Apoptotic markers (cleaved Caspase-3, BAX, PARP) were reduced, while BCL-2 was upregulated. Key miRNAs involved in steroidogenic and apoptotic regulation (miR-21, miR-22, miR-23b, miR-145, miR-199a) were enriched in primed sEVs.

CONCLUSION

Primed AMSC-sEVs offer a promising nanotherapeutic strategy to restore ovarian cell function in POI-like conditions via enhanced anti-apoptotic and steroidogenic effects. These findings support the translational potential of Primed sEVs for fertility preservation and the management of menopausal hormone deficiency, including early-stage ovarian insufficiency and genitourinary syndrome of menopause.

摘要

背景

卵巢早衰(POI)的特征是颗粒细胞(GC)功能障碍、类固醇生成减少和雌激素缺乏,常继发于化疗。尽管再生医学取得了进展,但无细胞纳米疗法在POI治疗方面仍未得到充分探索。

目的

本研究在环磷酰胺(CTX)诱导的GC损伤模型中研究预处理的禽间充质干细胞衍生的小细胞外囊泡(预处理的AMSC-sEVs)的治疗效果,该模型模拟了与POI相关的激素功能障碍。

方法

使用Exoid TRPS和电泳迁移率平台对预处理的AMSC-sEVs进行粒径、浓度和zeta电位表征。在人颗粒细胞(hGCs)中对预处理的和未处理的AMSC-sEVs进行功能比较,评估细胞活力、凋亡、类固醇生成和卵巢功能相关基因表达。通过下一代测序和qRT-PCR评估miRNA含量。

结果

预处理的AMSC-sEVs呈现出更小、更均匀的尺寸分布,显著提高的颗粒浓度和更大的负zeta电位(平均-24.4 mV对-13.3 mV),表明胶体稳定性得到改善。在体外,预处理的sEVs剂量依赖性地增强hGC增殖,恢复CTX诱导的抗苗勒管激素(AMH)、促卵泡激素受体(FSHR)和黄体生成素受体(LHCGR)的抑制,并提高雌二醇和孕酮水平。凋亡标志物(裂解的半胱天冬酶-3、BAX、聚(ADP-核糖)聚合酶(PARP))减少,而B细胞淋巴瘤-2(BCL-2)上调。参与类固醇生成和凋亡调节的关键miRNA(miR-21、miR-22、miR-23b、miR-145、miR-199a)在预处理的sEVs中富集。

结论

预处理的AMSC-sEVs通过增强抗凋亡和类固醇生成作用,为在类似POI的情况下恢复卵巢细胞功能提供了一种有前景的纳米治疗策略。这些发现支持预处理的sEVs在生育力保存和绝经激素缺乏管理方面的转化潜力,包括早期卵巢功能不全和绝经泌尿生殖综合征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2307/12435526/8040ac589840/IJN-20-11099-g0001.jpg

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