Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures

被引:60
|
作者
Sacchetto, Claudia [1 ,2 ]
Vitiello, Libero [2 ,3 ]
de Windt, Leon J. [1 ]
Rampazzo, Alessandra [2 ]
Calore, Martina [1 ]
机构
[1] Univ Maastricht, Dept Mol Genet, Univ Singel 50, NL-6229 ER Maastricht, Netherlands
[2] Univ Padua, Dept Biol, Via Ugo Bassi 58B, I-35131 Padua, Italy
[3] Adm Headquarters Univ Perugia, Interuniv Inst Myol IIM, Piazza Lucio Severi 1, I-06132 Perugia, Italy
基金
欧洲研究理事会;
关键词
cardiac disease modeling; human induced pluripotent stem cells; 3D cardiac models; engineered heart tissue; PLURIPOTENT STEM-CELL; ENGINEERED HUMAN MYOCARDIUM; CARDIAC MICROTISSUES; QT SYNDROME; FUNCTIONAL MATURATION; METABOLIC MATURATION; ENDOTHELIAL-CELLS; IMPROVE RECOVERY; TISSUE; CARDIOMYOPATHY;
D O I
10.3390/ijms21093404
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
In the last decade, the generation of cardiac disease models based on human-induced pluripotent stem cells (hiPSCs) has become of common use, providing new opportunities to overcome the lack of appropriate cardiac models. Although much progress has been made toward the generation of hiPSC-derived cardiomyocytes (hiPS-CMs), several lines of evidence indicate that two-dimensional (2D) cell culturing presents significant limitations, including hiPS-CMs immaturity and the absence of interaction between different cell types and the extracellular matrix. More recently, new advances in bioengineering and co-culture systems have allowed the generation of three-dimensional (3D) constructs based on hiPSC-derived cells. Within these systems, biochemical and physical stimuli influence the maturation of hiPS-CMs, which can show structural and functional properties more similar to those present in adult cardiomyocytes. In this review, we describe the latest advances in 2D- and 3D-hiPSC technology for cardiac disease mechanisms investigation, drug development, and therapeutic studies.
引用
收藏
页数:32
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