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ID 68247
フルテキストURL
fulltext.pdf 1.37 MB
著者
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
抄録
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.
キーワード
sinoatrial node
HCN channels
induced pluripotent stem cell
発行日
2024-12-11
出版物タイトル
Cells
13巻
24号
出版者
MDPI
開始ページ
2045
ISSN
2073-4409
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2024 by the authors.
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.3390/cells13242045
ライセンス
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
助成機関名
Japan Society for the Promotion of Science
助成番号
JP16K19407