A fully defined static suspension culture system for large-scale human embryonic stem cell production

被引:22
作者
Li, Xia [1 ,2 ,3 ]
Ma, Ruoyu [1 ,2 ,3 ]
Gu, Qi [2 ,4 ]
Liang, Lingmin [1 ,2 ,3 ]
Wang, Lei [1 ,2 ,3 ]
Zhang, Ying [1 ]
Wang, Xianning [1 ,2 ,3 ]
Liu, Xin [1 ,2 ,3 ]
Li, Zhongwen [1 ,2 ,3 ]
Fang, Jinhui [1 ,3 ]
Wu, Jun [1 ,3 ]
Wang, Yukai [1 ,3 ]
Li, Wei [1 ,2 ,3 ]
Hu, Baoyang [1 ,2 ]
Wang, Liu [1 ,2 ,3 ]
Zhou, Qi [1 ,2 ,3 ]
Hao, Jie [1 ,3 ]
机构
[1] Chinese Acad Sci, Inst Zool, State Key Lab Stem Cell & Reprod Biol, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Beijing Stem Cell Bank, Beijing 100190, Peoples R China
[4] Chinese Acad Sci, Inst Zool, State Key Lab Membrane Biol, Beijing 100101, Peoples R China
来源
CELL DEATH & DISEASE | 2018年 / 9卷
关键词
SCALABLE EXPANSION; ROCK INHIBITOR; HUMAN FEEDERS; DIFFERENTIATION; 3D; CRYOPRESERVATION; BIOREACTOR; GENERATION; DERIVATION; POLYMERS;
D O I
10.1038/s41419-018-0863-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human embryonic stem cells (hESCs) play an important role in regenerative medicine due to their potential to differentiate into various functional cells. However, the conventional adherent culture system poses challenges to mass production of high-quality hESCs. Though scientists have made many attempts to establish a robust and economical hESC suspension culture system, there are existing limitations, including suboptimal passage methods and shear force caused by dynamic stirring. Here, we report on an efficient large-scale culture system, which enables long-term, GMP grade, single-cell inoculation, and serial expansion of hESCs with a yield of about 1.5 x 10(9) cells per 1.5-L culture, while maintaining good pluripotency. The suspension culture system was enlarged gradually from a 100-mm dish to a 1.8-L culture bag with methylcellulose involvement to avoid sphere fusion. Under the optimal experimental protocol, this 3D system resolves current problems that limit mass production and clinical application of hESCs, and thus can be used in commercial-level hESC production for cell therapy and pharmaceutics screening in the future.
引用
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页数:9
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