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作 者:王毓斌[1] 陈斌[1] 王颖超[2] 张志玲[3] 王鸿祥[1] 卢永宁[1] 向祖琼[1] 胡凯[1] 杨怡珂[3] 韩银发[1] 汪铮[2] 王益鑫[1] 黄翼然[1]
机构地区:[1]上海交通大学医学院附属仁济医院,泌尿外科,上海市男科学研究所,上海200001 [2]上海交通大学医学院附属仁济医院,上海市消化疾病研究所干细胞实验室,上海200001 [3]上海交通大学医学院附属仁济医院,妇产科,上海200001
出 处:《中华男科学杂志》2008年第12期1063-1068,共6页National Journal of Andrology
基 金:上海市计划生育委员会科研基金(2007JG06)
摘 要:目的:探讨人精原干细胞分离、纯化及以人胚胎成纤维细胞为饲养层培养的方法和条件。方法:利用两步酶法和Percoll不连续密度离心法分离、纯化人精原干细胞,在人胚胎成纤维细胞饲养层上培养;用免疫组织化学方法检测精原干细胞表面标志SSEA-1和OCT4;检测精原干细胞克隆碱性磷酸酶活性;逆转录聚合酶链反应(RT-PCR)检测精原干细胞相关基因的表达。结果:精原干细胞在人胚胎成纤维细胞饲养层上可以存活并增殖形成集落。集落未分化标志检测显示SSEA-l、OCT4呈阳性,碱性磷酸酶活性呈强阳性,并表达精原干细胞相关基因。结论:人胚胎成纤维细胞饲养层可以支持人精原干细胞的生长。Objective: To investigate the methods and conditions for the isolation, purification and culture of human spermatogonial stem cells (SSCs) on the feeder layer cells of human embryonic fibroblasts (hEFs). Methods: SSCs isolated and purified from normal human fetal testicular tissues by sequential two-step enzyme digestion and Percoll uncontinuous density gradient centrifugation were cultured on the feeder layer cells of hEFs isolated from 5-9 weeks old human embryos. The surface markers SSEA-1 and OCT4 of the SSCs were detected by immunohistochemistry; the alkaline phosphatase (AKP) activity of the SSC clones measured; and the expressions of the SSC-related genes determined by RT-PCR. Results: SSCs survived, proliferated and formed colonies on the feeder layers, and the colonies were highly positive for SSEA-1 and OCT4, with strong AKP activity and high expressions of the SSC-related genes. Conclusion : The feeder layer of hEFs supports the growth of human spermatogonial stem cells.
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