Abstract
Specific cell lineages differentiated from human induced pluripotent stem cells (iPSCs) are promising sources for cell replacement therapy and are useful biomedical research tools for research on disease mechanisms and drug discovery. Among the different lineages, cardiac lineage has been one of the most efficiently differentiated through several established protocols. In this chapter, we describe our reproducible and highly efficient methodology for differentiating iPSCs into cardiomyocytes using embryoid bodies. We also describe methods to dissociate iPSC-derived cardiomyocytes and to evaluate iPSC-derived cardiomyocytes.
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Burridge PW, Keller G, Gold JD et al (2012) Production of de novo cardiomyocytes: human pluripotent stem cell differentiation and direct reprogramming. Cell Stem Cell 10:16–28
Mummery CL, Zhang J, Ng ES et al (2012) Differentiation of human embryonic stem cells and induced pluripotent stem cells to cardiomyocytes: a methods overview. Circ Res 111:344–358
Protze SI, Liu J, Nussinovitch U et al (2017) Sinoatrial node cardiomyocytes derived from human pluripotent cells function as a biological pacemaker. Nat Biotechnol 35:56–68
Lee JH, Protze SI, Laksman Z et al (2017) Human pluripotent stem cell-derived atrial and ventricular cardiomyocytes develop from distinct mesoderm populations. Cell Stem Cell 21:179–194.e4
Yang L, Soonpaa MH, Adler ED et al (2008) Human cardiovascular progenitor cells develop from a KDR+ embryonic-stem-cell-derived population. Nature 453:524–528
Kattman SJ, Witty AD, Gagliardi M et al (2011) Stage-specific optimization of activin/nodal and BMP signaling promotes cardiac differentiation of mouse and human pluripotent stem cell lines. Cell Stem Cell 8:228–240
Willems E, Spiering S, Davidovics H et al (2011) Small-molecule inhibitors of the Wnt pathway potently promote cardiomyocytes from human embryonic stem cell-derived mesoderm. Circ Res 109:360–364
Dubois NC, Craft AM, Sharma P et al (2011) SIRPA is a specific cell-surface marker for isolating cardiomyocytes derived from human pluripotent stem cells. Nat Biotechnol 29:1011–1018
Elliott DA, Braam SR, Koutsis K et al (2011) NKX2-5(eGFP/w) hESCs for isolation of human cardiac progenitors and cardiomyocytes. Nat Methods 8:1037–1040
Miki K, Endo K, Takahashi S et al (2015) Efficient detection and purification of cell populations using synthetic MicroRNA switches. Cell Stem Cell 16:699–711
Funakoshi S, Miki K, Takaki T et al (2016) Enhanced engraftment, proliferation, and therapeutic potential in heart using optimized human iPSC-derived cardiomyocytes. Sci Rep 6:19111
Acknowledgments
We greatly appreciate colleagues at our laboratories and the Department of Cardiovascular Medicine, Kyoto University. We thank Gordon Keller, Mark Gagliardi, Shunsuke Funakoshi, and Chikako Okubo for providing valuable advice and support for the differentiation method of cardiomyocytes, Ikue Takei, Misato Nishikawa, Azusa Inagaki, and Megumi Narita for technical support, and Peter Karagiannis for proofediting. We would like to express our heartfelt gratitude to Yoko Uematsu for her administrative support.
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Hatani, T., Miki, K., Yoshida, Y. (2018). Induction of Human Induced Pluripotent Stem Cells to Cardiomyocytes Using Embryoid Bodies. In: Ishikawa, K. (eds) Experimental Models of Cardiovascular Diseases. Methods in Molecular Biology, vol 1816. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-8597-5_6
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DOI: https://doi.org/10.1007/978-1-4939-8597-5_6
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