In vitro mouse preantral follicle development in 2D and suspension culture: α-MEM vs SAGE 1-step.

IF 3.4 Q2 REPRODUCTIVE BIOLOGY
Amir Bazgir, Narges Karami, Fatemeh Hassani, Farah Farokhi, Azam Dalman
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引用次数: 0

Abstract

Abstract: The in vitro culture of immature follicles remains a challenge in reproductive biology, ART, and fertility preservation. This study investigated the impact of α-MEM and SAGE 1-Step media on mouse preantral follicle development and oocyte maturation using two-dimensional (2D) and suspension culture systems. Preantral follicles (∼130 μm) from 14-day-old NMRI mice were cultured for 13 days in either medium under 2D or suspension conditions. On day 13, hCG was added to induce meiotic resumption. We evaluated follicular growth, antrum formation, oocyte maturation, meiotic spindle organization, and expression of genes related to maturation (Bmp15, Gdf9), cumulus expansion (Has2, Ptgs2, Lhr, Adamts1), and apoptosis (Bax, Bcl2). Antral formation was higher in α-MEM in both culture systems (P > 0.05). However, SAGE 1-Step significantly improved oocyte maturation across both systems (P = 0.01 in 2D vs P = 0.006 in suspension compared to α-MEM). Spindle staining demonstrated that suspension culture significantly increased the percentage of oocytes with normal meiotic spindle organization (P = 0.002). Gene expression analysis revealed a significant upregulation of Adamts1 (P = 0.008) and downregulation of Bax (P = 0.01) in suspension culture. Furthermore, the apoptotic ratio of Bax/Bcl2 was significantly decreased in the suspension system (P = 0.01). In conclusion, the SAGE 1-Step medium significantly enhances oocyte maturation, while the suspension system superiorly preserves meiotic spindle architecture and reduces apoptosis. The combination of SAGE 1-Step and suspension culture provides an optimized microenvironment for producing high-quality oocytes.

Lay summary: Growing immature egg outside the body, a process known as in vitro follicle culture, is a promising but challenging technique for preserving fertility. This study investigated novel approaches to improve this process, aiming to create healthier, more viable eggs for future use. The researchers found that using a specific medium significantly improved egg development and maturation. Importantly, they found that culturing these immature eggs in suspension, where the follicles remained floating in the medium, rather than in a traditional two-dimensional system where follicles inevitably flatten and partially lose their three-dimensional structure, resulted in significantly better outcomes. Eggs grown in suspension showed more organized cellular structures and reduced cell death compared to those cultured on a flat surface. These findings represent an important step toward reliably producing healthy, developmentally competent eggs outside the body, offering new hope for fertility preservation and assisted reproduction.

体外小鼠腔前卵泡2D和悬浮培养发育:α-MEM与SAGE 1-Step。
摘要:未成熟卵泡的体外培养在生殖生物学、ART和生育能力保存方面仍然是一个挑战。本研究采用二维(2D)和悬浮培养体系研究了α-MEM和SAGE 1-Step培养基对小鼠腔前卵泡发育和卵母细胞成熟的影响。将14日龄NMRI小鼠的腔前卵泡(~ 130µm)在2D或悬浮条件下培养13天。第13天,添加hCG诱导减数分裂恢复。我们评估了卵泡生长、窦腔形成、卵母细胞成熟、减数分裂纺锤体组织以及成熟相关基因(Bmp15、Gdf9)、积云扩张(Has2、Ptgs2、Lhr、Adamts1)和细胞凋亡(Bax、Bcl2)的表达。两种培养体系中α-MEM的形成均较高(P < 0.05)。然而,与α-MEM相比,SAGE 1-Step显著改善了两种系统中的卵母细胞成熟(与α-MEM相比,2D中P= 0.01,悬浮中P=0.006)。纺锤体染色显示悬浮培养显著增加了正常减数分裂纺锤体组织的卵母细胞百分比(P=0.002)。基因表达分析显示,悬浮培养中Adamts1表达上调(P=0.008), Bax表达下调(P=0.01)。此外,悬浮体系中Bax/Bcl2的凋亡比例显著降低(P=0.01)。综上所述,SAGE 1-Step培养基能显著促进卵母细胞成熟,而悬浮体系则能很好地保留减数分裂纺锤体结构并减少细胞凋亡。SAGE 1-Step和悬浮培养的结合为生产高质量的卵母细胞提供了优化的微环境。在体外培养未成熟的卵子,这一过程被称为体外卵泡培养,是一种有前途但具有挑战性的保持生育能力的技术。这项研究探索了改进这一过程的新方法,旨在为未来的使用创造更健康、更有活力的卵子。研究人员发现,使用一种特殊的培养基,可以显著改善卵子的发育和成熟。重要的是,他们发现在悬浮培养基中培养这些未成熟的卵子,其中卵泡保持漂浮在培养基中,而不是在传统的二维系统中,卵泡不可避免地变平并部分失去其三维结构,结果明显更好。与在平面上培养的卵子相比,在悬浮中生长的卵子显示出更有组织的细胞结构和更少的细胞死亡。这些资金代表着在体外可靠地产生健康、发育正常的卵子的重要一步,为保存生育能力和辅助生殖提供了新的希望。推进生育保存:在实验室中,一种特殊的培养基悬浮培养显著提高未成熟卵母细胞的质量。
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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