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通过免疫磁珠分选法分离人胚胎癌干细胞。

Isolation of human embryonal carcinoma stem cells by immunomagnetic sorting.

作者信息

Przyborski S A

机构信息

Department Biological Sciences, University of Durham, South Road, Durham DH1 3LE, United Kingdom.

出版信息

Stem Cells. 2001;19(6):500-4. doi: 10.1634/stemcells.19-6-500.

Abstract

Embryonal carcinoma cells are pluripotent stem cells derived from germ cell tumors and can be used to study cell differentiation in vitro. This report describes an approach designed to isolate pluripotent stem cells from primary/parent stock cultures of explanted tumor material. Cells expressing the pluripotent stem cell marker, SSEA-3, were isolated from heterogeneous stock cultures of the human teratoma line, TERA2, using immunomagnetic isolation. Single cell selection was performed on isolated SSEA-3+ cells and clonal lines were established. Each line was ultimately grown as a homogeneous monolayer, independent of feeder cells and expressed high levels of markers for pluripotent stem cells. In response to retinoic acid, clone TERA2.cl.SP-12 cells displayed enhanced neural differentiation compared to previously isolated TERA2 sublines and formed both neurons and glia. Deriving human pluripotent stem cell lines that differentiate into a range of cell types will provide useful tools to understand the molecular mechanisms controlling cell differentiation in a manner pertinent to human embryonic development.

摘要

胚胎癌细胞是源自生殖细胞肿瘤的多能干细胞,可用于体外研究细胞分化。本报告描述了一种从外植肿瘤材料的原代/亲本培养物中分离多能干细胞的方法。使用免疫磁珠分离法,从人畸胎瘤细胞系TERA2的异质培养物中分离出表达多能干细胞标志物SSEA-3的细胞。对分离出的SSEA-3+细胞进行单细胞选择,并建立克隆系。每个细胞系最终都作为均匀的单层生长,不依赖饲养细胞,并表达高水平的多能干细胞标志物。与先前分离的TERA2亚系相比,克隆TERA2.cl.SP-12细胞在视黄酸的作用下表现出增强的神经分化,并形成神经元和神经胶质细胞。获得能够分化为多种细胞类型的人多能干细胞系,将为以与人类胚胎发育相关的方式理解控制细胞分化的分子机制提供有用的工具。

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