ID 68247
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Vo, Quan Duy Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Nakamura, Kazufumi Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID publons researchmap
Saito, Yukihiro Department of Cardiovascular Medicine, Okayama University Hospital
Iida, Toshihiro Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Yoshida, Masashi Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID
Amioka, Naofumi Department of Cardiovascular Medicine, Okayama University Hospital
Akagi, Satoshi Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences ORCID Kaken ID
Miyoshi, Toru Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences ORCID Kaken ID publons
Yuasa, Shinsuke Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Abstract
Induced pluripotent stem cell (iPSC)-derived biological pacemakers have emerged as an alternative to traditional electronic pacemakers for managing cardiac arrhythmias. While effective, electronic pacemakers face challenges such as device failure, lead complications, and surgical risks, particularly in children. iPSC-derived pacemakers offer a promising solution by mimicking the sinoatrial node's natural pacemaking function, providing a more physiological approach to rhythm control. These cells can differentiate into cardiomyocytes capable of autonomous electrical activity, integrating into heart tissue. However, challenges such as achieving cellular maturity, long-term functionality, and immune response remain significant barriers to clinical translation. Future research should focus on refining gene-editing techniques, optimizing differentiation, and developing scalable production processes to enhance the safety and effectiveness of these biological pacemakers. With further advancements, iPSC-derived pacemakers could offer a patient-specific, durable alternative for cardiac rhythm management. This review discusses key advancements in differentiation protocols and preclinical studies, demonstrating their potential in treating dysrhythmias.
Keywords
sinoatrial node
HCN channels
induced pluripotent stem cell
Published Date
2024-12-11
Publication Title
Cells
Volume
volume13
Issue
issue24
Publisher
MDPI
Start Page
2045
ISSN
2073-4409
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2024 by the authors.
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PubMed ID
DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.3390/cells13242045
License
https://creativecommons.org/licenses/by/4.0/
Citation
Vo, Q.D.; Nakamura, K.; Saito, Y.; Iida, T.; Yoshida, M.; Amioka, N.; Akagi, S.; Miyoshi, T.; Yuasa, S. iPSC-Derived Biological Pacemaker—From Bench to Bedside. Cells 2024, 13, 2045. https://doi.org/10.3390/cells13242045
Funder Name
Japan Society for the Promotion of Science
助成番号
JP16K19407