SIRPA is a specific cell-surface marker for isolating cardiomyocytes derived from human pluripotent stem cells

被引:373
作者
Dubois, Nicole C. [1 ]
Craft, April M. [1 ]
Sharma, Parveen [2 ]
Elliott, David A. [3 ]
Stanley, Edouard G. [3 ]
Elefanty, Andrew G. [3 ]
Gramolini, Anthony [2 ]
Keller, Gordon [1 ]
机构
[1] Univ Hlth Network, Ontario Canc Inst, McEwen Ctr Regenerat Med, Toronto, ON, Canada
[2] Univ Toronto, Dept Physiol, Toronto, ON, Canada
[3] Monash Univ, Monash Immunol & Stem Cell Labs, Clayton, Vic, Australia
基金
英国医学研究理事会;
关键词
SIGNAL-REGULATORY PROTEIN; DIFFERENTIATION; TRANSPLANTATION; ACTIVATION; SCAFFOLD; SHPS-1; CD47;
D O I
10.1038/nbt.2005
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
To identify cell-surface markers specific to human cardiomyocytes, we screened cardiovascular cell populations derived from human embryonic stem cells (hESCs) against a panel of 370 known CD antibodies. This screen identified the signal-regulatory protein alpha (SIRPA) as a marker expressed specifically on cardiomyocytes derived from hESCs and human induced pluripotent stem cells (hiPSCs), and PECAM, THY1, PDGFRB and ITGA1 as markers of the nonmyocyte population. Cell sorting with an antibody against SIRPA allowed for the enrichment of cardiac precursors and cardiomyocytes from hESC/hiPSC differentiation cultures, yielding populations of up to 98% cardiac troponin T-positive cells. When plated in culture, SIRPA-positive cells were contracting and could be maintained over extended periods of time. These findings provide a simple method for isolating populations of cardiomyocytes from human pluripotent stem cell cultures, and thereby establish a readily adaptable technology for generating large numbers of enriched cardiomyocytes for therapeutic applications.
引用
收藏
页码:1011 / U82
页数:9
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