TY - JOUR
T1 - Therapeutic approaches for cardiac regeneration and repair
AU - Hashimoto, Hisayuki
AU - Olson, Eric N.
AU - Bassel-Duby, Rhonda
N1 - Funding Information:
The authors thank L. Amoasii and Y.-L. Min (University of Texas Southwestern Medical Center, USA) and S. Tohyama (Keio University School of Medicine, Japan) for constructive scientific discussions, J. Cabrera (University of Texas Southwestern Medical Center, USA) for assistance with figures, and A. McKenzie (University of Texas Southwestern Medical Center, USA) for help with editing. Work in the authors’ laboratory is supported by grants from the NIH (AR-067294, HL-130253, HD-087351, and HL-138426), Fondation Leducq Transatlantic Networks of Excellence in Cardiovascular Research, and the Robert A. Welch Foundation (grant 1–0025 to E.N.O.). H.H. is supported by the Uehara Memorial Foundation Postdoctoral Fellowship and the Kanae Foreign Study Grant.
Publisher Copyright:
© 2018, Macmillan Publishers Ltd., part of Springer Nature.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - Ischaemic heart disease is a leading cause of death worldwide. Injury to the heart is followed by loss of the damaged cardiomyocytes, which are replaced with fibrotic scar tissue. Depletion of cardiomyocytes results in decreased cardiac contraction, which leads to pathological cardiac dilatation, additional cardiomyocyte loss, and mechanical dysfunction, culminating in heart failure. This sequential reaction is defined as cardiac remodelling. Many therapies have focused on preventing the progressive process of cardiac remodelling to heart failure. However, after patients have developed end-stage heart failure, intervention is limited to heart transplantation. One of the main reasons for the dramatic injurious effect of cardiomyocyte loss is that the adult human heart has minimal regenerative capacity. In the past 2 decades, several strategies to repair the injured heart and improve heart function have been pursued, including cellular and noncellular therapies. In this Review, we discuss current therapeutic approaches for cardiac repair and regeneration, describing outcomes, limitations, and future prospects of preclinical and clinical trials of heart regeneration. Substantial progress has been made towards understanding the cellular and molecular mechanisms regulating heart regeneration, offering the potential to control cardiac remodelling and redirect the adult heart to a regenerative state.
AB - Ischaemic heart disease is a leading cause of death worldwide. Injury to the heart is followed by loss of the damaged cardiomyocytes, which are replaced with fibrotic scar tissue. Depletion of cardiomyocytes results in decreased cardiac contraction, which leads to pathological cardiac dilatation, additional cardiomyocyte loss, and mechanical dysfunction, culminating in heart failure. This sequential reaction is defined as cardiac remodelling. Many therapies have focused on preventing the progressive process of cardiac remodelling to heart failure. However, after patients have developed end-stage heart failure, intervention is limited to heart transplantation. One of the main reasons for the dramatic injurious effect of cardiomyocyte loss is that the adult human heart has minimal regenerative capacity. In the past 2 decades, several strategies to repair the injured heart and improve heart function have been pursued, including cellular and noncellular therapies. In this Review, we discuss current therapeutic approaches for cardiac repair and regeneration, describing outcomes, limitations, and future prospects of preclinical and clinical trials of heart regeneration. Substantial progress has been made towards understanding the cellular and molecular mechanisms regulating heart regeneration, offering the potential to control cardiac remodelling and redirect the adult heart to a regenerative state.
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U2 - 10.1038/s41569-018-0036-6
DO - 10.1038/s41569-018-0036-6
M3 - Review article
C2 - 29872165
AN - SCOPUS:85048057711
SN - 1759-5002
VL - 15
SP - 585
EP - 600
JO - Nature Reviews Cardiology
JF - Nature Reviews Cardiology
IS - 10
ER -