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Review
. 2021 Dec;95(12):3633-3650.
doi: 10.1007/s00204-021-03172-3. Epub 2021 Oct 17.

Recent progress of iPSC technology in cardiac diseases

Affiliations
Review

Recent progress of iPSC technology in cardiac diseases

Shunsuke Funakoshi et al. Arch Toxicol. 2021 Dec.

Abstract

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.

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

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Conflict of interest statement

YY received research funding from Takeda Pharmaceutical Company, Ltd.

Figures

Fig. 1
Fig. 1
Generation of iPSC cardiomyocytes and their application to cardiovascular diseases
Fig. 2
Fig. 2
Subtype differentiation of iPSCs and platforms to model diseases
Fig. 3
Fig. 3
In vitro maturation of iPSC cardiomyocytes by mimicking the postnatal maturation process in vivo

References

    1. Andersen P, Tampakakis E, Jimenez DV, Kannan S, Miyamoto M, Shin HK, Saberi A, Murphy S, Sulistio E, Chelko SP, Kwon C. Precardiac organoids form two heart fields via bmp/wnt signaling. Nat Commun. 2018;9:3140. doi: 10.1038/s41467-018-05604-8. - DOI - PMC - PubMed
    1. Ando H, Yoshinaga T, Yamamoto W, Asakura K, Uda T, Taniguchi T, Ojima A, Shinkyo R, Kikuchi K, Osada T, Hayashi S, Kasai C, Miyamoto N, Tashibu H, Yamazaki D, Sugiyama A, Kanda Y, Sawada K, Sekino Y. A new paradigm for drug-induced torsadogenic risk assessment using human ips cell-derived cardiomyocytes. J Pharmacol Toxicol Methods. 2017;84:111–127. doi: 10.1016/j.vascn.2016.12.003. - DOI - PubMed
    1. Arrowsmith J, Miller P. Trial watch: phase ii and phase iii attrition rates 2011–2012. Nat Rev Drug Discov. 2013;12:569. doi: 10.1038/nrd4090. - DOI - PubMed
    1. Ashrafian H, Redwood C, Blair E, Watkins H. Hypertrophic cardiomyopathy: a paradigm for myocardial energy depletion. Trends Genet. 2003;19:263–268. doi: 10.1016/S0168-9525(03)00081-7. - DOI - PubMed
    1. Baek M, DiMaio F, Anishchenko I, Dauparas J, Ovchinnikov S, Lee GR, Wang J, Cong Q, Kinch LN, Schaeffer RD, Millan C, Park H, Adams C, Glassman CR, DeGiovanni A, Pereira JH, Rodrigues AV, van Dijk AA, Ebrecht AC, Opperman DJ, Sagmeister T, Buhlheller C, Pavkov-Keller T, Rathinaswamy MK, Dalwadi U, Yip CK, Burke JE, Garcia KC, Grishin NV, Adams PD, Read RJ, Baker D. Accurate prediction of protein structures and interactions using a three-track neural network. Science. 2021;373:871–876. doi: 10.1126/science.abj8754. - DOI - PMC - PubMed

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