Recent progress of iPSC technology in cardiac diseases.
Shunsuke FunakoshiYoshinori YoshidaPublished in: Archives of toxicology (2021)
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.
Keyphrases
- induced pluripotent stem cells
- endothelial cells
- end stage renal disease
- cell therapy
- drug induced
- cardiovascular disease
- chronic kidney disease
- induced apoptosis
- liver injury
- prognostic factors
- pluripotent stem cells
- stem cells
- high throughput
- cell cycle arrest
- peritoneal dialysis
- heart failure
- coronary artery disease
- bone marrow
- mesenchymal stem cells
- human health
- cell proliferation
- atrial fibrillation
- patient reported
- cardiovascular risk factors
- climate change
- current status
- single cell
- pi k akt