Development of scalable culture systems for human embryonic stem cells

被引:38
作者
Azarin, Samira M. [1 ,2 ]
Palecek, Sean P. [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Chem & Biol Engn, Madison, WI 53706 USA
[2] WiCell Res Inst, Madison, WI 53707 USA
基金
美国国家科学基金会;
关键词
Human embryonic stem cells; Culture scale-up; Bioreactors; SELF-RENEWAL; GROWTH-FACTOR; MAINTAINS PLURIPOTENCY; WNT/BETA-CATENIN; DIFFERENTIATION; PROLIFERATION; DERIVATION; MATRICES; SPHINGOSINE-1-PHOSPHATE; MAINTENANCE;
D O I
10.1016/j.bej.2009.10.020
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The use of human pluripotent stem cells, including embryonic and induced pluripotent stem cells, in therapeutic applications will require the development of robust, scalable culture technologies for undifferentiated cells. Advances made in large-scale cultures of other mammalian cells will facilitate expansion of undifferentiated human embryonic stem cells (hESCs), but challenges specific to hESCs will also have to be addressed, including development of defined, humanized culture media and substrates, monitoring spontaneous differentiation and heterogeneity in the cultures, and maintaining karyotypic integrity in the cells. This review will describe our current understanding of environmental factors that regulate hESC self-renewal and efforts to provide these cues in various scalable bioreactor culture systems. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:378 / 384
页数:7
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