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Cryopreserved mouse fetal liver stromal cells treated with mitomycin C are able to support the growth of human embryonic stem cells

机译:丝裂霉素C处理的冷冻保存的小鼠胎儿肝基质细胞能够支持人类胚胎干细胞的生长

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摘要

An immortalized mouse fetal liver stromal cell line, named KM3, has demonstrated the potential to support the growth and maintenance of human embryonic stem cells (hESCs). In this study, the characteristics of KM3 cells were examined following cryopreservation at −70°C and in liquid nitrogen for 15, 30 and 60 days following treatment with 10 μg/ml mitomycin C. In addition, whether the KM3 cells were suitable for use as feeder cells to support the growth of hESCs was evaluated. The inhibition of mitosis without cell death was observed when the KM3 cells were treated with 10 μg/ml mitomycin C for 2 h. The morphology of the KM3 cells cryopreserved in liquid nitrogen for 60 days was not markedly changed, and the cell survival rate was 84.60±1.14%. By contrast, the survival rate of the KM3 cells was 66.40±2.88% following cryopreservation at −70°C for 60 days; the cells readily detached, were maintained for a shorter time, and had a reduced expression level of basic fibroblast growth factor. hESCs cultured on KM3 cells cryopreserved in liquid nitrogen for 60 days showed the typical bird’s nest structure, with clear boundaries and a differentiation rate of 16.33±2.08%. The differentiation rate of hESCs cultured on KM3 cells cryopreserved at −70°C for 60 days was 37.67±3.51%. These results indicate that the cryopreserved KM3 cells treated with mitomycin C may be directly used in the subculture of hESCs, and the effect is relatively good with −70°C short-term or liquid nitrogen cryopreservation.
机译:永生化的小鼠胎儿肝基质细胞系,称为KM3,已证明有潜力支持人类胚胎干细胞(hESCs)的生长和维持。在这项研究中,在用70μg/ ml丝裂霉素C处理后,在-70°C和液氮中冷冻保存15、30和60天后,检查了KM3细胞的特性。此外,KM3细胞是否适合使用评估了支持hESCs生长的饲养细胞。当用10μg/ ml丝裂霉素C处理KM3细胞2小时时,观察到有丝分裂抑制作用而无细胞死亡。在液氮中冷冻保存60天的KM3细胞的形态没有明显改变,细胞存活率为84.60±1.14%。相反,在-70°C冷冻保存60天后,KM3细胞的存活率为66.40±2.88%。细胞容易脱落,维持时间较短,碱性成纤维细胞生长因子的表达水平降低。在液氮中冷冻保存60天的KM3细胞上培养的hESCs具有典型的鸟巢结构,边界清晰,分化率为16.33±2.08%。在−70°C下冷冻保存60天的KM3细胞上培养的hESCs的分化率为37.67±3.51%。这些结果表明,用丝裂霉素C处理的冷冻保存的KM3细胞可以直接用于hESCs的继代培养,并且在-70°C短期或液氮冷冻保存中效果相对较好。

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