胚状体
胚胎干细胞
诱导多能干细胞
细胞生物学
生物
干细胞
细胞培养
细胞分化
继代培养(生物学)
分子生物学
遗传学
微生物学
基因
作者
Mi‐Young Son,Hyun‐Jin Kim,Minjeong Kim,Yee Sook Cho
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2011-05-03
卷期号:6 (5): e19134-e19134
被引量:30
标识
DOI:10.1371/journal.pone.0019134
摘要
Spherical three-dimensional cell aggregates called embryoid bodies (EBs), have been widely used in in vitro differentiation protocols for human pluripotent stem cells including human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs). Recent studies highlight the new devices and techniques for hEB formation and expansion, but are not involved in the passaging or subculture process. Here, we provide evidence that a simple periodic passaging markedly improved hEB culture condition and thus allowed the size-controlled, mass production of human embryoid bodies (hEBs) derived from both hESCs and hiPSCs. hEBs maintained in prolonged suspension culture without passaging (>2 weeks) showed a progressive decrease in the cell growth and proliferation and increase in the apoptosis compared to 7-day-old hEBs. However, when serially passaged in suspension, hEB cell populations were significantly increased in number while maintaining the normal rates of cell proliferation and apoptosis and the differentiation potential. Uniform-sized hEBs produced by manual passaging using a 1∶4 split ratio have been successfully maintained for over 20 continuous passages. The passaging culture method of hEBs, which is simple, readily expandable, and reproducible, could be a powerful tool for improving a robust and scalable in vitro differentiation system of human pluripotent stem cells.
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