| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2039281 | Cell Reports | 2015 | 13 Pages |
•Telomerase hyperactivation is an early event during zebrafish heart regeneration•Telomerase loss of function impairs cardiac regeneration•The proliferative response of cardiomyocytes is inhibited in tert−/− zebrafish•Telomerase protects cardiac cells from DNA damage and limits cellular senescence
SummaryAfter myocardial infarction in humans, lost cardiomyocytes are replaced by an irreversible fibrotic scar. In contrast, zebrafish hearts efficiently regenerate after injury. Complete regeneration of the zebrafish heart is driven by the strong proliferation response of its cardiomyocytes to injury. Here we show that, after cardiac injury in zebrafish, telomerase becomes hyperactivated, and telomeres elongate transiently, preceding a peak of cardiomyocyte proliferation and full organ recovery. Using a telomerase-mutant zebrafish model, we found that telomerase loss drastically decreases cardiomyocyte proliferation and fibrotic tissue regression after cryoinjury and that cardiac function does not recover. The impaired cardiomyocyte proliferation response is accompanied by the absence of cardiomyocytes with long telomeres and an increased proportion of cardiomyocytes showing DNA damage and senescence characteristics. These findings demonstrate the importance of telomerase function in heart regeneration and highlight the potential of telomerase therapy as a means of stimulating cell proliferation upon myocardial infarction.
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