iPSC-Derived Cardiomyocytes in Inherited Cardiac Arrhythmias: Pathomechanistic Discovery and Drug Development

被引:4
作者
Simons, Eline [1 ,2 ]
Loeys, Bart [1 ,2 ]
Alaerts, Maaike [1 ,2 ]
机构
[1] Univ Antwerp, Ctr Med Genet, Cardiogenet Res Grp, B-2650 Antwerp, Belgium
[2] Antwerp Univ Hosp, B-2650 Antwerp, Belgium
基金
欧洲研究理事会;
关键词
iPSC; cardiac arrhythmia; iPSC-derived cardiomyocytes; LONG-QT SYNDROME; PLURIPOTENT STEM-CELLS; POLYMORPHIC VENTRICULAR-TACHYCARDIA; BRUGADA SYNDROME; I-KR; PATIENT; MODEL; RESCUES; MATURATION; PHENOTYPE;
D O I
10.3390/biomedicines11020334
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
With the discovery of induced pluripotent stem cell (iPSCs) a wide range of cell types, including iPSC-derived cardiomyocytes (iPSC-CM), can now be generated from an unlimited source of somatic cells. These iPSC-CM are used for different purposes such as disease modelling, drug discovery, cardiotoxicity testing and personalised medicine. The 2D iPSC-CM models have shown promising results, but they are known to be more immature compared to in vivo adult cardiomyocytes. Novel approaches to create 3D models with the possible addition of other (cardiac) cell types are being developed. This will not only improve the maturity of the cells, but also leads to more physiologically relevant models that more closely resemble the human heart. In this review, we focus on the progress in the modelling of inherited cardiac arrhythmias in both 2D and 3D and on the use of these models in therapy development and drug testing.
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页数:20
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