用于前房卵泡长期多重发育的生物工程三维卵巢模型:为聚(ε-己内酯)(PCL)基支架的生殖应用搭建桥梁

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Reproductive Biology and Endocrinology Pub Date : 2024-08-02 DOI:10.1186/s12958-024-01266-y
Chiara Di Berardino, Alessia Peserico, Chiara Camerano Spelta Rapini, Liliana Liverani, Giulia Capacchietti, Valentina Russo, Paolo Berardinelli, Irem Unalan, Andrada-Ioana Damian-Buda, Aldo R Boccaccini, Barbara Barboni
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引用次数: 0

摘要

背景:辅助生殖技术(ART)已在人类和动物身上得到验证,可解决不孕、衰老、基因选择/扩增和疾病等生殖问题。辅助生殖技术在生物医学应用方面的长期空白在于重现卵巢卵泡生成的早期阶段,从而提供驱动大量储备未成熟卵泡进入促性腺激素依赖阶段的方案。组织工程正成为可能重现卵巢结构的具体解决方案,主要依赖于在天然或合成支架上使用自体早期卵泡。基于这些前提,本研究旨在验证使用聚(ε-己内酯)(PCL)制造的卵巢生物启发图案电纺纤维支架在多个前胚叶(PA)卵泡发育中的应用:方法:在 PCL 支架上培养从羔羊卵巢中分离出的 PA 卵泡,培养方法既可采用有效的单卵泡培养方案(Ctrl),也可模拟多卵泡培养条件,即在人工卵巢中移植 5 个或 10 个 PA(AO5PA 和 AO10PA)。在评估基于支架的微环境对体外卵泡生成(ivF)和卵子生成在形态和功能层面的适宜性之前,分别进行了14天和18天的培养:结果:体外卵泡生成结果表明,PCL支架可生成适当的仿生卵巢微环境,通过支持卵泡生长和类固醇生成活化,支持多PA卵泡向早期前叶(EA)阶段过渡。此外,通过提高减数分裂能力、大染色质重塑和孤雌生殖发育能力,长期进行的PCL-多倍体生物工程ivF(AO10PA)产生了最大比例的高度特化配子:该研究展示了使用 PCL 模板支架进行下一代 ART 的概念验证,该支架旨在生成移植自体早期卵泡的可移植人工卵巢,或利用三维生物启发基质促进生理性长期多 PA 卵泡方案,从而推动人工受孕技术的发展。
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Bioengineered 3D ovarian model for long-term multiple development of preantral follicle: bridging the gap for poly(ε-caprolactone) (PCL)-based scaffold reproductive applications.

Background: Assisted Reproductive Technologies (ARTs) have been validated in human and animal to solve reproductive problems such as infertility, aging, genetic selection/amplification and diseases. The persistent gap in ART biomedical applications lies in recapitulating the early stage of ovarian folliculogenesis, thus providing protocols to drive the large reserve of immature follicles towards the gonadotropin-dependent phase. Tissue engineering is becoming a concrete solution to potentially recapitulate ovarian structure, mostly relying on the use of autologous early follicles on natural or synthetic scaffolds. Based on these premises, the present study has been designed to validate the use of the ovarian bioinspired patterned electrospun fibrous scaffolds fabricated with poly(ε-caprolactone) (PCL) for multiple preantral (PA) follicle development.

Methods: PA follicles isolated from lamb ovaries were cultured on PCL scaffold adopting a validated single-follicle protocol (Ctrl) or simulating a multiple-follicle condition by reproducing an artificial ovary engrafted with 5 or 10 PA (AO5PA and AO10PA). The incubations were protracted for 14 and 18 days before assessing scaffold-based microenvironment suitability to assist in vitro folliculogenesis (ivF) and oogenesis at morphological and functional level.

Results: The ivF outcomes demonstrated that PCL-scaffolds generate an appropriate biomimetic ovarian microenvironment supporting the transition of multiple PA follicles towards early antral (EA) stage by supporting follicle growth and steroidogenic activation. PCL-multiple bioengineering ivF (AO10PA) performed in long term generated, in addition, the greatest percentage of highly specialized gametes by enhancing meiotic competence, large chromatin remodeling and parthenogenetic developmental competence.

Conclusions: The study showcased the proof of concept for a next-generation ART use of PCL-patterned scaffold aimed to generate transplantable artificial ovary engrafted with autologous early-stage follicles or to advance ivF technologies holding a 3D bioinspired matrix promoting a physiological long-term multiple PA follicle protocol.

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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.
期刊最新文献
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