胚胎干细胞
碱性成纤维细胞生长因子
细胞生物学
纤维连接蛋白
科斯尔
成纤维细胞
细胞培养
生物
干细胞
成纤维细胞生长因子
免疫学
生长因子
细胞外基质
成体干细胞
遗传学
受体
基因
作者
Michal Amit,Joseph Itskovitz‐Eldor
出处
期刊:Methods in Enzymology
日期:2006-01-01
卷期号:: 37-49
被引量:64
标识
DOI:10.1016/s0076-6879(06)20003-x
摘要
In addition to their contribution to research fields such as early human development, self-renewal, and differentiation mechanisms, human embryonic stem cells (hESCs) may serve as a tool for drug testing and for the study of cell-based therapies. Traditionally, these cells have been cultured with mouse embryonic fibroblast (MEF) feeder layers, which allow their continuous growth in an undifferentiated state. However, for future clinical applications, hESCs should be cultured under defined conditions, preferably in a xeno-free culture system, where exposure to animal pathogens is prevented. To this end, different culture methods for hESCs, based on serum replacement and free of supportive cell layers, were developed. This chapter discusses a simple, feeder-free culture system on the basis of medium supplemented with transforming growth factor beta1 (TGFbeta1), basic fibroblast growth factor (bFGF) and fibronectin as matrix.
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