微载波
实验室烧瓶
胚胎干细胞
细胞培养
细胞生物学
生物技术
人诱导多能干细胞
干细胞
诱导多能干细胞
再生医学
化学定义介质
生物
化学
生化工程
体外
生物化学
工程类
遗传学
基因
物理化学
作者
Paulo André Marinho,Daniel Tait Vareschini,Ismael C. Gomes,Bruna Paulsen,Daniel Rodrigues Furtado,Leda dos Reis Castilho,Stevens K. Rehen
出处
期刊:Tissue Engineering Part C-methods
[Mary Ann Liebert, Inc.]
日期:2012-07-27
卷期号:19 (2): 146-155
被引量:37
标识
DOI:10.1089/ten.tec.2012.0141
摘要
Currently, stem cell research faces a major bottleneck related to the low efficiency of methods to produce large quantities of human embryonic stem cells (ESC) for use in clinical trials. Most culture media currently employed for human ESC cultivation contain animal compounds, and cells are grown in static flasks. Besides the immediate contamination with nonhuman compounds, cell expansion in flasks tends to be laborious and nonefficient. Here we cultured human ESC in stirred microcarrier (MC) systems using an animal/human-component-free medium, to overcome both issues. The method developed to culture cells on suspended beads combined the use of polymeric MCs in stirred vessels with an optimized culture medium free of supplements of animal and human origin. This approach generated approximately 160 million cells within 6 days, which were shown to remain pluripotent. The process developed herein provides a step forward toward therapy due to the economic advantages in the production of human ESC and to their consequent low immunogenic potential.
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