作者: Daniel J. Garry , Mary G. Garry , Andre Klaassen Kamdar , Forum Kamdar , Naoko Koyano-Nakagawa
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摘要: Inherited cardiomyopathies, including hypertrophic cardiomyopathy, dilated arrythmogenic right ventricular and other inherited forms of heart failure, represent a unique set genetically defined cardiovascular disease processes. Unraveling the molecular mechanisms these deadly human has been challenging, but recent groundbreaking scientific advances in stem cell technology have allowed for generation patient-specific inducible (hiPSC)ederived cardiomyocytes (CMs). hiPSC-derived CMs retain genetic blueprint patient, they can be maintained culture, recapitulate phenotypic characteristics vitro, thus serving as dish. This review provides an overview vitro modeling cardiomyopathies with use CMs. (J Cardiac Fail 2015;21:761e770)