Xiao Zhun, Wang Yan, Li Ling-Ling, Li Shang-wei
Reproductive Medical Center of West China 2nd University Hospital, Sichuan University, Chengdu 610041, China.
Department of Obstetrics and Gynecology of Sichuan Provincial Hospital for Women and Children, Chengdu 610031, China.
Cryo Letters. 2013 Sep-Oct;34(5):520-6.
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 < 0.05). 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.
本研究的目的是确定针浸玻璃化法(NIV)是否能提高解冻后卵巢组织体外培养的生长潜能。使用NIV和慢速冷冻法对人卵巢皮质组织进行冷冻保存。培养14天后,用光镜对NIV组和慢速冷冻组的保存结果进行组织学分析,并用TUNEL法评估细胞凋亡情况。结果显示,NIV组形态异常的原始卵泡百分比低于慢速冷冻组(P<0.05)。NIV组TUNEL阳性原始卵泡的发生率低于慢速冷冻组(P<0.05)。该研究表明,用NIV冷冻保存人卵巢组织可有效提高冻融后卵巢组织体外培养的生长潜能。