TY - JOUR
T1 - Production of functional cardiomyocytes and cardiac tissue from human induced pluripotent stem cells for regenerative therapy
AU - Tani, Hidenori
AU - Tohyama, Shugo
AU - Kishino, Yoshikazu
AU - Kanazawa, Hideaki
AU - Fukuda, Keiichi
N1 - Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2022/3
Y1 - 2022/3
N2 - The emergence of human induced pluripotent stem cells (hiPSCs) has revealed the potential for curing end-stage heart failure. Indeed, transplantation of hiPSC-derived cardiomyocytes (hiPSC-CMs) may have applications as a replacement for heart transplantation and conventional regenerative therapies. However, there are several challenges that still must be overcome for clinical applications, including large-scale production of hiPSCs and hiPSC-CMs, elimination of residual hiPSCs, purification of hiPSC-CMs, maturation of hiPSC-CMs, efficient engraftment of transplanted hiPSC-CMs, development of an injection device, and avoidance of post-transplant arrhythmia and immunological rejection. Thus, we developed several technologies based on understanding of the metabolic profiles of hiPSCs and hiPSC derivatives. In this review, we outline how to overcome these hurdles to realize the transplantation of hiPSC-CMs in patients with heart failure and introduce cutting-edge findings and perspectives for future regenerative therapy.
AB - The emergence of human induced pluripotent stem cells (hiPSCs) has revealed the potential for curing end-stage heart failure. Indeed, transplantation of hiPSC-derived cardiomyocytes (hiPSC-CMs) may have applications as a replacement for heart transplantation and conventional regenerative therapies. However, there are several challenges that still must be overcome for clinical applications, including large-scale production of hiPSCs and hiPSC-CMs, elimination of residual hiPSCs, purification of hiPSC-CMs, maturation of hiPSC-CMs, efficient engraftment of transplanted hiPSC-CMs, development of an injection device, and avoidance of post-transplant arrhythmia and immunological rejection. Thus, we developed several technologies based on understanding of the metabolic profiles of hiPSCs and hiPSC derivatives. In this review, we outline how to overcome these hurdles to realize the transplantation of hiPSC-CMs in patients with heart failure and introduce cutting-edge findings and perspectives for future regenerative therapy.
KW - Cardiomyocyte
KW - Induced pluripotent stem cell
KW - Maturation
KW - Metabolism
KW - Regenerative therapy
KW - Spheroid
KW - Transplantation
UR - http://www.scopus.com/inward/record.url?scp=85120420812&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85120420812&partnerID=8YFLogxK
U2 - 10.1016/j.yjmcc.2021.11.008
DO - 10.1016/j.yjmcc.2021.11.008
M3 - Article
C2 - 34822838
AN - SCOPUS:85120420812
SN - 0022-2828
VL - 164
SP - 83
EP - 91
JO - Journal of Molecular and Cellular Cardiology
JF - Journal of Molecular and Cellular Cardiology
ER -