Propagation of human embryonic and induced pluripotent stem cells in an indirect co-culture system

被引:12
作者
Abraham, Sheena [2 ]
Sheridan, Steven D. [1 ,3 ]
Laurent, Louise C. [4 ,5 ]
Albert, Kelsey [2 ]
Stubban, Christopher [6 ]
Ulitsky, Igor [7 ]
Miller, Bradley [8 ]
Loring, Jeanne F. [1 ,6 ]
Rao, Raj R. [2 ]
机构
[1] MIT, Dept Brain & Cognit Sci, Picower Inst Learning & Memory, Cambridge, MA 02139 USA
[2] Virginia Commonwealth Univ, Richmond, VA USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Human Genet Res, Boston, MA USA
[4] Scripps Res Inst, Ctr Regenerat Med, La Jolla, CA 92037 USA
[5] Univ Calif San Diego, San Diego, CA 92103 USA
[6] Burnham Inst Med Res, La Jolla, CA USA
[7] Tel Aviv Univ, Sch Comp Sci, Tel Aviv, Israel
[8] Univ Virginia, Dept Pathol, Charlottesville, VA 22903 USA
基金
以色列科学基金会; 美国国家科学基金会;
关键词
Human pluripotent stem cells; Microporous membranes; Indirect co-culture; Cell separation; CULTURE; DIFFERENTIATION; LINES;
D O I
10.1016/j.bbrc.2010.01.101
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have developed and validated a microporous poly(ethylene terephthalate) membrane-based indirect co-culture system for human pluripotent stem cell (hPSC) propagation, which allows real-time conditioning of the culture medium with human fibroblasts while maintaining the complete separation of the two cell types. The propagation and pluripotent characteristics of a human embryonic stem cell (hESC) line and a human induced pluripotent stem cell (hiPSC) line were studied in prolonged culture in this system. We report that hPSCs cultured on membranes by indirect co-culture with fibroblasts were indistinguishable by multiple criteria from hPSCs cultured directly on a fibroblast feeder layer. Thus this co-culture system is a significant advance in hPSC culture methods, providing a facile stem cell expansion system with continuous medium conditioning while preventing mixing of hPSCs and feeder cells. This membrane culture method will enable testing of novel feeder cells and differentiation studies using co-culture with other cell types, and will simplify stepwise changes in culture conditions for staged differentiation protocols. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:211 / 216
页数:6
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