Abstract
Purpose of Review
Many forms of heart disease result in the essentially irreversible loss of cardiomyocytes. The ability to promote cardiomyocyte renewal may be a promising approach to reverse injury in diseased hearts. The purpose of this review is to describe the impact of cardiomyocyte cell cycle activation on cardiac function and structure in several different models of myocardial disease.
Recent Findings
Transgenic mice expressing cyclin D2 (D2 mice) exhibit sustained cardiomyocyte renewal in the adult heart. Earlier studies demonstrated that D2 mice exhibited progressive myocardial regeneration in experimental models of myocardial infarction, and that cardiac function was normalized to values seen in sham-operated litter mates by 180 days post-injury. D2 mice also exhibited markedly improved atrial structure in a genetic model of atrial fibrosis. More recent studies revealed that D2 mice were remarkably resistant to heart failure induced by chronic elevated afterload as compared with their wild type (WT siblings), with a 6-fold increase in median survival as well as retention of relatively normal cardiac function. Finally, D2 mice exhibited a progressive recovery in cardiac function to normal levels and a concomitant reduction in adverse myocardial remodeling in an anthracycline cardiotoxicity model.
Summary
The studies reviewed here make a strong case for the potential utility of inducing cardiomyocyte renewal as a means to treat injured hearts. Several challenges which must be met to develop a viable therapeutic intervention based on these observations are discussed.
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Arash Eghbali and Austin Dukes contributed equally to this work.
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Arash Eghbali, Austin Dukes, Karl Toischer, and Loren J. Field declare that they have no conflict of interest.
Gerd Hasenfuss reports personal fees from Corvia, Servier, Impulse Dynamics, Novartis, AstraZeneca, Vifor Pharma, Berlin Chemie, and Springer.
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Eghbali, A., Dukes, A., Toischer, K. et al. Cell Cycle–Mediated Cardiac Regeneration in the Mouse Heart. Curr Cardiol Rep 21, 131 (2019). https://doi.org/10.1007/s11886-019-1206-9
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DOI: https://doi.org/10.1007/s11886-019-1206-9