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Two Methods of Vitrification Followed by In Vitro Culture of the Ovine Ovary: Evaluation of the Follicular Development and Ovarian Extracellular Matrix

机译:绵羊卵巢体外培养的两种玻璃化方法:卵泡发育和卵巢细胞外基质的评估

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Contents The aim of this study was to evaluate the influence of two vitrification techniques on the extra cellular matrix (ECM) and ovarian follicular development. The ovarian cortex was fragmented (9mm(3)) and divided into six groups, viz. fresh control, cultured control, vitrified by the Ovarian Tissue Cryosystem (OTC) method, conventional solid surface vitrification (SSV) method, OTC/cultured and SSV/cultured. Follicles from all the fragments were analysed for morphology, development and viability. The ECM was evaluated based on the condition of collagen and reticular fibres and the immunolocalization of type I collagen and fibronectin. After 7days of culture, the tissue vitrified by OTC revealed a higher percentage (p0.05) of morphologically normal (30.66%) and viable (60.00%) follicles when compared with those vitrified using the SSV technique (21.33% and 23.00%). In all the fragments cultured, regardless of the vitrification method, a significantly higher percentage of developing follicles was observed when compared with the non-cultured tissue. Analysis of the type I collagen showed increased immunostaining after the in vitro culture in the vitrified fragments. In conclusion, the OTC is better for preserving the follicular viability and morphology and maintaining the integrity of the extracellular matrix components of the ovine ovary.
机译:内容这项研究的目的是评估两种玻璃化技术对细胞外基质(ECM)和卵巢滤泡发育的影响。卵巢皮质被碎片化(9mm(3))并分为六组,即。新鲜控制,培养控制,通过卵巢组织冷冻系统(OTC)方法玻璃化,常规固体表面玻璃化(SSV)方法,OTC /培养和SSV /培养。分析所有片段中的卵泡的形态,发育和生存力。根据胶原蛋白和网状纤维的状况以及I型胶原蛋白和纤连蛋白的免疫定位来评估ECM。培养7天后,与使用SSV技术进行玻璃化处理的卵泡相比,通过OTC玻璃化处理的组织显示出较高的形态正常卵泡(30.66%)和可存活卵泡(60.00%)的百分比(p <0.05)。与未培养的组织相比,在所有培养的片段中,无论采用何种玻璃化方法,均观察到显着更高的发育卵泡百分比。对I型胶原的分析显示,在玻璃化片段的体外培养后,免疫染色增加。总之,OTC可以更好地保存卵泡的生存力和形态,并保持绵羊卵巢细胞外基质成分的完整性。

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