家猫玻璃化卵母细胞的卵泡样环境。

M. Colombo, M. Morselli, G. Luvoni
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摘要

玻璃化卵母细胞(VOs)的体外发育仍然不是最理想的(Mandawala等,2016),传统的二维(2D)培养系统可能不足以充分利用VOs的潜力。利用三维(3D)卵泡样结构,即颗粒细胞(GCs)和半透性3D基质的结合,可以模拟生理微环境,促进VOs成熟和胚胎发育。本研究的目的是评估在三维海藻酸钡微胶囊(卵泡状结构)中包裹的GCs与在二维单层中培养的GCs相比的类固醇生成能力(雌二醇和孕酮分泌)以及在这些系统中培养的VOs的成熟结果。纯化后(Simsek & Arikan, 2015),从离体卵巢中提取的cat GCs在3D微胶囊(Vigo et al., 2005)或2D单层中体外培养6天。第2天和第6天收集条件培养基,采用酶联荧光法测定激素水平。同一天,将3D和2D培养的GCs作为人工环境,对Cryotop方案获得的VOs进行体外成熟。采用双苯并胺染色法测定核成熟度。在三维卵泡样结构和二维单层结构中观察到甾体形成;激素浓度随时间增加而增加,第6天各系统间差异显著(p=0.02)。玻璃化卵母细胞在培养2天的GCs存在下恢复减数分裂(3D: 45.5%;2D: 56.7%),而培养6天的GCs显著阻碍了单层VOs减数分裂的进展(21.7%,p=0.007),但支持滤泡样结构的高比例完全成熟(26.7%,p=0.07)。三维微胶囊中的颗粒细胞保持了其生理特征,这些卵泡样结构能够恢复VOs的发育能力。然而,VOs培养方法的进一步发展将优化这些宝贵资源的利用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Follicle-like environment for domestic cat vitrified oocytes.
The in vitro development of vitrified oocytes (VOs) is still suboptimal (Mandawala et al., 2016) and the traditional two-dimensional (2D) culture systems might not be adequate to fully exploit VOs potential. The use of three-dimensional (3D) follicle-like structures, i.e. a combination of granulosa cells (GCs) and semipermeable 3D matrices, could mimic the physiological microenvironment and enhance VOs maturation and embryo development.The aim of this study was to assess the steroidogenic ability (estradiol and progesterone secretion) of GCs encapsulated in 3D barium alginate microcapsules (follicle-like structure) compared to GCs cultured in a 2D monolayer and the maturation outcomes of VOs cultured in these systems.After purification (Simsek & Arikan, 2015), cat GCs retrieved from isolated ovaries were in vitro cultured for 6 days in 3D microcapsules (Vigo et al., 2005) or in 2D monolayers. On days 2 and 6, conditioned medium was collected and hormonal determination by enzyme-linked fluorescent assay was performed. On the same days, 3D and 2D cultured GCs were used as artificial milieu for in vitro maturation of VOs obtained by Cryotop protocol. Nuclear maturation was assessed by bis-benzimide staining.Steroidogenesis was observed in 3D follicle-like structures as well as in 2D monolayers; hormonal concentration increased over time and on day 6 it significantly differed between systems (p=0.02). Vitrified oocytes resumed meiosis in presence of GCs cultured for 2 days (3D: 45.5%; 2D: 56.7%), while GCs cultured for 6 days significantly hindered VOs meiosis progression in monolayers (21.7%, p=0.007), but supported high proportions of full maturation in follicle-like structures (26.7%, p=0.07).Granulosa cells in 3D microcapsules maintained their physiological features and these follicle-like structures were able to restore VOs developmental abilities. However, further advancements in VOs culture methods would optimize the use of these valuable resources.
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