Cardiomyocyte differentiation of pluripotent stem cells and their use as cardiac disease models

被引:55
作者
Dambrot, Cheryl [1 ,2 ]
Passier, Robert [1 ]
Atsma, Douwe [2 ]
Mummery, Christine L. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Anat & Embryol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Cardiol, NL-2300 RC Leiden, Netherlands
关键词
cardiac disease model; cardiac differentiation; cardiomyocyte; drug discovery; pluripotent stem cell; regenerative medicine; ZINC-FINGER NUCLEASES; HUMAN FIBROBLASTS; ROCK INHIBITOR; SELF-RENEWAL; FUNCTIONAL CARDIOMYOCYTES; UNDIFFERENTIATED GROWTH; MAINTAIN PLURIPOTENCY; GENETIC MANIPULATION; GENERATION; EFFICIENT;
D O I
10.1042/BJ20101707
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
More than 10 years after their first isolation, human embryonic stem cells are finally 'coming of age' in research and biotechnology applications as protocols for their differentiation and undifferentiated expansion in culture become robust and scalable, and validated commercial reagents become available. Production of human cardiomyocytes is now feasible on a daily basis for many laboratories with tissue culture expertise. An additional recent surge of interest resulting from the first production of human iPSCs (induced pluripotent stem cells) from somatic cells of patients now makes these technologies of even greater importance since it is likely that (genetic) cardiac disease phenotypes can be captured in the cardiac derivatives of these cells. Although cell therapy based on replacing cardiomyocytes lost or dysfunctional owing to cardiac disease are probably as far away as ever, biotechnology and pharmaceutical applications in safety pharmacology and drug discovery will probably impact this clinical area in the very near future. In the present paper, we review the cutting edge of this exciting area of translational research.
引用
收藏
页码:25 / 35
页数:11
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