Cardiomyocytes purified from differentiated embryonic stem cells exhibit characteristics of early chamber myocardium

被引:69
作者
Fijnvandraat, AC
van Ginneken, ACG
Schumacher, CA
Boheler, KR
Deprez, RHL
Christoffels, VM
Moorman, AFM
机构
[1] Univ Amsterdam, Dept Anat & Embryol, Acad Med Ctr, Expt & Mol Cardiol Grp, NL-1105 AZ Amsterdam, Netherlands
[2] NIA, Cardiovasc Sci Lab, NIH, Baltimore, MD 21224 USA
关键词
embryonic stem cells; in vitro differentiation; transcription factors; chamber formation; genetic selection; Ncx1; ANEPPS;
D O I
10.1016/j.yjmcc.2003.09.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mouse embryonic stem (ES) cells easily differentiate towards the cardiac lineage making them suitable as an in vitro model to study cardiogenesis and as a potential source of transplantable cells. In this study, we show by in situ hybridisation that about 30% of the volume of cultures of differentiating ES cells consists of cardiomyocytes. RT-PCR analyses showed that the transcription factors Nkx2.5, Gata4, Mef2c and Irx4 were expressed at levels in the same order of magnitude as the levels observed in embryonic, neonatal and adult hearts. Atrial natriuretic factor and Connexin 40, associated with chamber formation in vivo, are expressed at relatively low levels, similar to those observed at early heart development in vivo. To facilitate the isolation of ES cell-derived cardiomyocytes, a cell line was constructed by stable transfection of the aminoglycoside phosphotransferase cDNA driven by the cardiac-specific distant upstream part of the Na+/Ca2+ exchanger promoter. To accomplish single-copy integration, the construct was inserted into the hypoxanthine phosphoribosyltransferase locus of HMI ES cells by homologous recombination. Cardiac-specific resistance to G418-sulphate (neomycin) allowed isolation of a pure population of cardiomyocytes. Genetically selected and unselected cell populations were characterised electrophysiologically using patch clamp. To explore whether clusters of cells have a similar differentiation profile, action potentials (APs) were measured in aggregates of differentiating ES cells, using a new method based on the voltage-dependent fluorescent dye di-4-ANEPPS. Both whole-cell recordings using patch-clamp and optical measurements with di-4-ANEPPS of the AP showed that upstroke velocity increases and AP duration decreases with differentiation time, accompanied by a decrease in AP interval, suggesting the initiation of the developmental programme underlying the formation of chamber myocardium. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1461 / 1472
页数:12
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