4.7 Review

Recent progress of iPSC technology in cardiac diseases

Journal

ARCHIVES OF TOXICOLOGY
Volume 95, Issue 12, Pages 3633-3650

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00204-021-03172-3

Keywords

Induced pluripotent stem cells; Cardiomyocyte; Disease modeling; Maturation; Differentiation into subtypes

Categories

Funding

  1. JSPS KAKENHI [17H04176, 21H02912]
  2. Research Center Network for Realization of Regenerative Medicine, Japan Agency for Medical Research and Development (AMED) [JP19bm0104001, JP19bm0204003, JP19bm0804008, JP20bm0804022]
  3. Research on Regulatory Science of Pharmaceuticals and Medical Devices, AMED [JP19mk0104117]
  4. Research Project for Practical Applications of Regenerative Medicine, AMED [JP19bk0104095]
  5. Leducq Foundation [18CVD05]
  6. iPS Cell Research Fund
  7. Grants-in-Aid for Scientific Research [21H02912, 17H04176] Funding Source: KAKEN

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Over the past nearly 15 years, advancements in differentiation methods related to induced pluripotent stem cells have provided new opportunities and platforms for research and treatment of cardiovascular diseases.
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.

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