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Human umbilical cord stem cell conditioned medium versus serum-free culture medium in the treatment of cryopreserved human ovarian tissues in in-vitro culture: a randomized controlled trial

机译:人脐带干细胞条件培养基与无血清培养基在体外培养中冷冻保存的人卵巢组织的治疗:一项随机对照试验

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Background To reduce young female fertility loss, the in-vitro culture of cryopreserved ovarian cortical tissues (OCTs) is considered an effective approach without delaying treatment and undergoing stimulation medicine. However, ischemic damage and follicular loss during the in-vitro culture of OCTs are major technical challenges. Human umbilical cord stem cells (HUMSCs) and their conditioned medium (HUMSC-CM) have been considered to be potential resources for regeneration medicine because they secrete cytokines and enhance cell survival and function. The aim of this study was to determine whether HUMSC-CM improves the development of frozen-thawed in-vitro cultured ovarian tissues compared with a serum-free culture medium (SF-CM). Methods The thawed OCTs ( n =?68) were cultivated in HUMSC-CM and SF-CM in vitro for 8?days, and the ovarian tissues were processed and analyzed by a classical histological evaluation. The microvessel density (MVD) and apotosis detection during in-vitro culture of OCTs were also performed. Results A significant difference in the rate of morphologically normal primordial follicles in the HUMSC-CM group was observed compared to that in the SF-CM group (group C) from days 2 to 4 (day 2: group B 58.0?±?2.45% vs group C 32.0?±?5.83%, p =?0.002; day 3: group B 55.5?±?4.20% vs group C 21.0?±?9.80%, p =?0.048; day 4: group B 52.0?±?4.08% vs group C 21.5?±?8.19%, p =?0.019). The microvessel density (MVD) detection showed a time-dependent increase and peaked on day 4. There was a significant difference between groups B (49.33?±?0.58) and C (24.33?±?3.79) ( p =?0.036). The percentage of apoptotic follicles in group B was lower than that in group C on day 1 (13.75?±?2.50% vs 27.0?±?10.10%, p =?0.003), day 5 (11.75?±?1.50% vs 51.0?±?10.5%, p =?0.019) and day 7 (15.0?±?5.10% vs 46.5?±?21.75%, p =?0.018). Conclusions These data have provided the first experimental evidence of the effect of HUMSC-CM on frozen-thawed OCTs in vitro. The results showed that the HUMSC-CM group provided a better protecting effect on the in-vitro culture of the cryopreserved OCTs compared to the SF-CM group.
机译:背景技术为了减少年轻女性的生育能力丧失,冷冻保存的卵巢皮质组织(OCT)的体外培养被认为是一种有效的方法,无需延迟治疗并接受刺激性药物。然而,OCT体外培养期间的缺血性损伤和滤泡损失是主要的技术挑战。人脐带血干细胞(HUMSCs)及其条件培养基(HUMSC-CM)被认为是再生医学的潜在资源,因为它们分泌细胞因子并增强细胞存活和功能。这项研究的目的是确定与无血清培养基(SF-CM)相比,HUMSC-CM是否能改善冻融的体外培养卵巢组织的发育。方法在HUMSC-CM和SF-CM中体外培养解冻的OCTs(n =?68)8天,并通过经典的组织学评价对卵巢组织进行处理和分析。还进行了OCT体外培养过程中的微血管密度(MVD)和细胞凋亡检测。结果从第2天到第4天(第2天:B组),HUMSC-CM组的形态正常原始卵泡率与SF-CM组(C组)相比有显着差异。相对于C组32.0%±5.83%,p = 0.002;第3天:B组55.5%±4.20%vs C组21.0%±9.80%,p = 0.048;第4天:B组52.0%±±0.04;相对于C组为21.5±±8.19%(4.08%),p =±0.019)。微血管密度(MVD)检测显示出时间依赖性增加,并在第4天达到峰值。B组(49.33±±0.58)和C组(24.33±±3.79)之间存在显着差异(p =±0.036)。第1天,B组的凋亡卵泡百分比低于C组(13.75±2.5.0%vs 27.0±10.10%,p = 0.003),第5天(11.75±1.50%vs 51.0)。 ?±10.5%,p = 0.019)和第7天(15.0±5.10%对46.5±21.75%,p = 0.018)。结论这些数据提供了HUMSC-CM对冻融OCT体外影响的第一个实验证据。结果表明,与SF-CM组相比,HUMSC-CM组对冷冻保存的OCT的体外培养具有更好的保护作用。

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