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Human induced pluripotent stem cells for studying mitochondrial diseases in the heart.

Arianne CaudalLu RenChengyi TuJoseph C Wu
Published in: FEBS letters (2022)
Mitochondrial dysfunction is known to contribute to a range of diseases, and primary mitochondrial defects strongly impact high-energy organs such as the heart. Platforms for high-throughput and human-relevant assessment of mitochondrial diseases are currently lacking, hindering the development of targeted therapies. In the past decade, human-induced pluripotent stem cells (iPSCs) have become a promising technology for drug discovery in basic and clinical research. In particular, human iPSC-derived cardiomyocytes (iPSC-CMs) offer a unique tool to study a wide range of mitochondrial functions and possess the potential to become a key translational asset for mitochondrial drug development. This review summarizes mitochondrial functions and recent therapeutic discoveries, advancements and limitations of using iPSC-CMs to study mitochondrial diseases of the heart with an emphasis on cardiac applications.
Keyphrases
  • induced pluripotent stem cells
  • oxidative stress
  • endothelial cells
  • drug discovery
  • atrial fibrillation
  • left ventricular
  • risk assessment