Human-Induced Pluripotent Stem Cell Technology and Cardiomyocyte Generation: Progress and Clinical Applications

被引:47
|
作者
Di Baldassarre, Angela [1 ]
Cimetta, Elisa [2 ]
Bollini, Sveva [3 ]
Gaggi, Giulia [1 ]
Ghinassi, Barbara [1 ]
机构
[1] Univ G dAnnunzio, Dept Med & Aging Sci, I-66100 Chieti, Italy
[2] Univ Padua, Dept Ind Engn DII, I-35131 Padua, Italy
[3] Univ Genoa, Dept Expt Med, Lab Regenerat Med, I-16121 Genoa, Italy
关键词
regenerative medicine; reprogramming; cardiac differentiation; secretoma; tissue engineering; DE-NOVO CARDIOMYOCYTES; IN-VITRO; CARDIAC MYOCYTES; CARDIOVASCULAR PROGENITORS; EPIGENETIC REGULATION; FUNCTIONAL-PROPERTIES; DIFFERENTIATION; HEART; MATURATION; EXPANSION;
D O I
10.3390/cells7060048
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human-induced pluripotent stem cells (hiPSCs) are reprogrammed cells that have hallmarks similar to embryonic stem cells including the capacity of self-renewal and differentiation into cardiac myocytes. The improvements in reprogramming and differentiating methods achieved in the past 10 years widened the use of hiPSCs, especially in cardiac research. hiPSC-derived cardiac myocytes (CMs) recapitulate phenotypic differences caused by genetic variations, making them attractive human disease models and useful tools for drug discovery and toxicology testing. In addition, hiPSCs can be used as sources of cells for cardiac regeneration in animal models. Here, we review the advances in the genetic and epigenetic control of cardiomyogenesis that underlies the significant improvement of the induced reprogramming of somatic cells to CMs; the methods used to improve scalability of throughput assays for functional screening and drug testing in vitro; the phenotypic characteristics of hiPSCs-derived CMs and their ability to rescue injured CMs through paracrine effects; we also cover the novel approaches in tissue engineering for hiPSC-derived cardiac tissue generation, and finally, their immunological features and the potential use in biomedical applications.
引用
收藏
页数:31
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