Arrhythmia Mechanisms in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes

被引:11
|
作者
Paci, Michelangelo [1 ]
Penttinen, Kirsi [1 ]
Pekkanen-Mattila, Mari [1 ]
Koivumaki, Jussi T. [1 ]
机构
[1] Tampere Univ, Fac Med & Hlth Technol, BioMediTech, Tampere, Finland
基金
芬兰科学院;
关键词
hiPSC-CM; arrhythmia mechanisms; in vitro; in silico; LONG-QT SYNDROME; POLYMORPHIC VENTRICULAR-TACHYCARDIA; JUNCTION PROTEIN PHENOTYPES; SUDDEN CARDIAC DEATH; TORSADE-DE-POINTES; PACE-MAKER CURRENT; HYPERTROPHIC CARDIOMYOPATHY; EARLY AFTERDEPOLARIZATIONS; DILATED CARDIOMYOPATHY; ACTION-POTENTIALS;
D O I
10.1097/FJC.0000000000000972
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite major efforts by clinicians and researchers, cardiac arrhythmia remains a leading cause of morbidity and mortality in the world. Experimental work has relied on combining high-throughput strategies with standard molecular and electrophysiological studies, which are, to a great extent, based on the use of animal models. Because this poses major challenges for translation, the progress in the development of novel antiarrhythmic agents and clinical care has been mostly disappointing. Recently, the advent of human induced pluripotent stem cell-derived cardiomyocytes has opened new avenues for both basic cardiac research and drug discovery; now, there is an unlimited source of cardiomyocytes of human origin, both from healthy individuals and patients with cardiac diseases. Understanding arrhythmic mechanisms is one of the main use cases of human induced pluripotent stem cell-derived cardiomyocytes, in addition to pharmacological cardiotoxicity and efficacy testing, in vitro disease modeling, developing patient-specific models and personalized drugs, and regenerative medicine. Here, we review the advances that the human induced pluripotent stem cell-derived-based modeling systems have brought so far regarding the understanding of both arrhythmogenic triggers and substrates, while also briefly speculating about the possibilities in the future.
引用
收藏
页码:300 / 316
页数:17
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