Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5604545 | International Journal of Cardiology | 2017 | 8 Pages |
Abstract
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, a more 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.
Keywords
GATA4SANNCXECMICMSMEF2CAPDHAND2VPAMYH7N2bcTnIcTNTIK1hiPSCsGATA binding protein 4c-jun amino-terminal kinasePSCsMYH6Myocyte enhancer factor 2CTbx5IRX4Cardiomyocyte maturationSarcoplasmic/endoplasmic reticulum Ca2+ ATPaseTGF-βhiPSC-CMsMLC2vNRVMsRMPRyR2hESCsFGFJnkVmaxIGF-1EHTIPSCsINaNeonatal rat ventricular myocytesNa+/Ca2+ exchangerCa2+-induced Ca2+ releaseengineered heart tissueTransforming Growth Factor Betacardiac troponin TTriiodothyroninesodium currentInward rectifier potassium currentaction potential amplitudeSarcoplasmic reticulummyosin heavy chain 7Hey1Stem cellsHuman induced pluripotent stem cellshuman embryonic stem cellsHuman induced pluripotent stem cell-derived cardiomyocytesInduced pluripotent stem cellsPluripotent stem cellsInsulin growth factor 1Vascular endothelial growth factorVascular Endothelial Growth Factor (VEGF)fibroblast growth factorOxidative phosphorylationSERCACardiomyocyteExtracellular matrixAction potential durationValproic acidaction potentialresting membrane potentialAPAVentricular cardiomyocyteconnexin 40Creatine kinaseCICRconnexin 43Sino-atrial nodeRyanodine receptor 2
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Authors
Tomasz J. Kolanowski, Christopher L. Antos, Kaomei Guan,