Recent progress of iPSC technology in cardiac diseases

被引:25
|
作者
Funakoshi, Shunsuke [1 ,2 ]
Yoshida, Yoshinori [1 ,2 ]
机构
[1] Kyoto Univ, Ctr iPS Cell Res & Applicat, Kyoto 6068507, Japan
[2] Takeda CiRA Joint Program T CiRA, Fujisawa, Kanagawa 2518555, Japan
关键词
Induced pluripotent stem cells; Cardiomyocyte; Disease modeling; Maturation; Differentiation into subtypes; PLURIPOTENT STEM-CELL; RIGHT-VENTRICULAR CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; DILATED CARDIOMYOPATHY; SIGNALING PROMOTES; PROGENITOR CELLS; STROMAL CELLS; CARDIOMYOCYTES; MATURATION; MODEL;
D O I
10.1007/s00204-021-03172-3
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
It has been nearly 15 years since the discovery of human-induced pluripotent stem cells (iPSCs). During this time, differentiation methods to targeted cells have dramatically improved, and many types of cells in the human body can be currently generated at high efficiency. In the cardiovascular field, the ability to generate human cardiomyocytes in vitro with the same genetic background as patients has provided a great opportunity to investigate human cardiovascular diseases at the cellular level to clarify the molecular mechanisms underlying the diseases and discover potential therapeutics. Additionally, iPSC-derived cardiomyocytes have provided a powerful platform to study drug-induced cardiotoxicity and identify patients at high risk for the cardiotoxicity; thus, accelerating personalized precision medicine. Moreover, iPSC-derived cardiomyocytes can be sources for cardiac cell therapy. Here, we review these achievements and discuss potential improvements for the future application of iPSC technology in cardiovascular diseases.
引用
收藏
页码:3633 / 3650
页数:18
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