The invention of the induced pluripotent stem cell (iPSC) technology allows patient-specific, mature somatic cells to be converted into an unlimited supply of pluripotent stem cells (PSCs). These iPSCs can then in turn be differentiated into any cell type including neurons, cardiac cells, pancreatic cells, liver cells, blood cells or enterocytes. Although cardiovascular disease (CVD) is a leading cause of death in the world, the limited cell derivation and cell number in cardiac tissue makes it difficult to study the CVDs using the existing cardiac cell model. By differentiating the patient-specific iPSCs into cardiomyocytes, scientists can generate iPSC-based 'disease in a dish' models and use them to better understand disease mechanism. Here we review the current progress in using iPSC-derived cardiomyocytes to model human CVDs.
Keyphrases
- induced apoptosis
- cardiovascular disease
- stem cells
- cell cycle arrest
- endothelial cells
- pluripotent stem cells
- single cell
- left ventricular
- cell therapy
- heart failure
- gene expression
- oxidative stress
- spinal cord
- magnetic resonance imaging
- signaling pathway
- magnetic resonance
- metabolic syndrome
- spinal cord injury
- cell proliferation
- genome wide
- living cells
- cardiovascular risk factors
- fluorescent probe