ID | 68247 |
フルテキストURL | |
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
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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
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Miyoshi, Toru
Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
ORCID
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Yuasa, Shinsuke
Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
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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.
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キーワード | sinoatrial node
HCN channels
induced pluripotent stem cell
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発行日 | 2024-12-11
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出版物タイトル |
Cells
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巻 | 13巻
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号 | 24号
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出版者 | MDPI
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開始ページ | 2045
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ISSN | 2073-4409
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資料タイプ |
学術雑誌論文
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言語 |
英語
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OAI-PMH Set |
岡山大学
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著作権者 | © 2024 by the authors.
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論文のバージョン | publisher
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PubMed ID | |
DOI | |
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関連URL | isVersionOf https://doi.org/10.3390/cells13242045
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ライセンス | https://creativecommons.org/licenses/by/4.0/
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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
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助成機関名 |
Japan Society for the Promotion of Science
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助成番号 | JP16K19407
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