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In vitro culture thawed human ovarian tissue: NIV versus slow freezing method

机译:体外培养融化的人卵巢组织:NIV与慢速冷冻方法

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摘要

The aim of this study was to determine if the needle immersed vitrification method (NIV) can improve the growth potential of thawed ovarian tissue in vitro culture. Human ovarian cortical tissues were cryopreserved using NIV and slow freezing method. After 14 days of culture, the preservation outcomes of NIV and slow freezing groups were analyzed histologically using light microscope and apoptosis was assessed by TUNEL assay. The result showed that the percentage of morphologically abnormal primordial follicles was lower in NIV group than in slow freezing group (P<.05). The incidence of TUNEL-positive primordial follicles was lower in NIV group than in slow freezing group (P<0.05). The study showed that cryopreservation of human ovarian tissue with NIV was effective in improving the growth potential of frozen-thawed ovarian tissue in vitro culture.
机译:这项研究的目的是确定针浸玻璃化法(NIV)是否可以提高体外培养的卵巢组织解冻的生长潜力。使用NIV和慢速冷冻方法将人卵巢皮质组织冷冻保存。培养14天后,使用光学显微镜对NIV和慢速冷冻组的保存结果进行组织学分析,并通过TUNEL测定评估细胞凋亡。结果表明,NIV组的形态异常原始卵泡百分比低于慢速冷冻组(P <0.05)。 NIV组的TUNEL阳性原始卵泡的发生率低于慢速冷冻组(P <0.05)。研究表明,用NIV冷冻保存人卵巢组织可有效提高体外培养的冻融卵巢组织的生长潜力。

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