Making human cardiomyocytes up to date: Derivation, maturation state and perspectives

被引:81
|
作者
Kolanowski, Tomasz J. [1 ]
Antos, Christopher L. [1 ,2 ]
Guan, Kaomei [1 ]
机构
[1] Tech Univ Dresden, Inst Pharmacol & Toxicol, Fetscherstr 74, D-01307 Dresden, Germany
[2] ShanghaiTech Univ, Sch Life Sci & Technol, 100 Haike Rd, Shanghai 201210, Peoples R China
关键词
Stem cells; Induced pluripotent stem cells; Cardiomyocyte derivation protocols; Cardiomyocyte maturation; In vitro derived-cardiomyocyte applications; CELL-DERIVED CARDIOMYOCYTES; PLURIPOTENT STEM-CELLS; ELECTRICAL-STIMULATION; ENGINEERED MYOCARDIUM; DIFFERENTIATION; FIBROBLASTS; SYSTEM; MODULATION; ACTIVATION; ENERGETICS;
D O I
10.1016/j.ijcard.2017.03.099
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In vitro generation of cardiomyocytes (CMs) from human cells opens the possibility to develop patient-specific therapies to various cardiomyopathies. By establishing the in vitro reprograming methods that produce human CMs, we learn about what is involved in the development of specific CM subtypes. In this review, we summarize the latest achievements in CM generation technologies, emphasizing the differentiation methods of specific CM subtypes. We also relate the biological properties and functions of the in vitro-generated CMs to those of their in vivo counterparts. Furthermore, we describe the main problem of current CM derivation methods - maturation of CMs. We subsequently discuss biochemical and physical stimuli that are used to overcome the maturation problems of in vitro-derived CMs. As a result, amore holistic approach with controllable environment and timing of specific stimuli for creation of more mature engineered heart tissues is described as well. Finally, we propose a novel approach in which enhancing energy transfer mechanisms in the immature CMs might help to overcome the current hurdle of incomplete in vitro differentiation. (C) 2017 The Authors. Published by Elsevier Ireland Ltd.
引用
收藏
页码:379 / 386
页数:8
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