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小鼠胚胎成纤维细胞的分离培养及饲养层制备
引用本文:胡三强,;王妍妍,;马永宾,;胡嘉波.小鼠胚胎成纤维细胞的分离培养及饲养层制备[J].中国临床康复,2014(45):7306-7311.
作者姓名:胡三强  ;王妍妍  ;马永宾  ;胡嘉波
作者单位:[1]连云港市妇幼保健院检验科,江苏省连云港市222000; [2]江苏大学医学院,江苏省镇江市212013
基金项目:江苏大学高级人才专项资助(09JDG037);国家自然科学基金资助项目(31071421)
摘    要:背景:建立一种既可以大量制备,又易于保存并保持较高活性的饲养层细胞是人胚胎干细胞培养研究的重要环节。 目的:建立昆明小鼠胚胎成纤维细胞的最佳分离培养方法,评价其用于人胚胎干细胞饲养层研究的可行性。方法:用不同浓度胰蛋白酶分步消化法体外分离和培养昆明小鼠胚胎成纤维细胞,观察其生物学特性,制备胚胎成纤维细胞饲养层,检测人胚胎干细胞在饲养层上培养的生长状态。〈br〉 结果与结论:制备昆明小鼠胚胎成纤维细胞饲养层的最佳胎龄为13.5 d。不同浓度胰蛋白酶分步消化法制备的胚胎成纤维细胞生长状态好,获得的成纤维细胞纯度高,增殖活跃。冻存2周,1,3,6个月内复苏的细胞存活率差异无显著性意义。小鼠胚胎成纤维细胞在第2-4代增殖旺盛,第5代以后细胞增殖活力明显下降。人胚胎干细胞在小鼠胚胎成纤维细胞长期传代后呈典型的未分化形态,碱性磷酸酶和过碘酸-雪夫染色均为阳性。结果表明建立的昆明小鼠胚胎成纤维细胞饲养层分离培养法可为人胚胎干细胞扩增提供稳定、优质的饲养层细胞。

关 键 词:干细胞  培养  人胚胎干细胞  小鼠胚胎成纤维细胞  饲养层  国家自然科学基金

Isolation and culture of mouse embryonic fibroblasts and preparation of feeder layers
Institution:Hu San-qiang, Wang Yan-yan, Ma Yong-bin, Hu Jia-bo (1Department of Clinical Laboratory, Lianyungang Maternal and Child Health Hospital, Lianyungang 222000, Jiangsu Province, China; 2 School of Medicine, Jiangsu University, Zhenjiang 212013, Jiangsu Province, China)
Abstract:BACKGROUND:It is important to produce and save a large amount of high-activity feeder cel s for the culture of human embryonic stem cel s. 〈br〉 OBJECTIVE:To establish the optimal method for isolation and culture of Kunming mouse embryonic fibroblasts, and to evaluate the feasibility of preparing feeder layers for culture of human embryonic stem cel s. 〈br〉 METHODS:Embryonic fibroblasts were isolated and cultured by different concentrations of trypsin from Kunming mouse fetuses in vitro. The biological characteristics and growth rule of mouse embryonic fibroblasts were investigated, and then the feeder layers for human embryonic stem cel s culture were produced. The growth of human embryonic stem cel s on the prepared feeder layer was tested. 〈br〉 RESULTS AND CONCLUSION:The optimal fetal age for preparing Kunming mouse embryonic fibroblast feeder layer was 13.5 days. Kunming mouse embryonic fibroblasts at different concentrations grew wel with high purity and active proliferation by trypsin digestion method. There was no significant difference in the survival rate of cel s after cryopreservation for 2 weeks, 1 month, 3 months and 6 months. The cel s were proliferative from the second to fourth passage and declined sharply after the fifth passage. Human embryonic stem cel s which grew on Kunming mouse embryonic fibroblasts feeder layers were stil to remain the typical undifferentiated morphology and were strongly positive for alkaline phosphatase and periodic acid-Schiff after long-term subculture. The 〈br〉 mouse embryonic fibroblasts can be used as the stable and high-quality feeder cel s for human embryonic stem cel s.
Keywords:embryonic stem cel s  fibroblasts  trophoblasts
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