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Oxidative phosphorylation is required for cardiomyocyte re-differentiation and long-term fish heart regeneration

Abstract:
In contrast to humans, fish can fully regenerate their hearts after cardiac injury. However, not all fish have the same regenerative potential, allowing comparative inter-species and intra-species analysis to identify the mechanisms controlling successful heart regeneration. Here we report a differential regenerative response to cardiac cryo-injury among different wild-type zebrafish strains. Correlating these data with single-cell and bulk RNA sequencing data, we identify oxidative phosphorylation (OXPHOS) as a positive regulator of long-term regenerative outcome. OXPHOS levels, driven by glycolysis through the malate-aspartate shuttle, increase as soon as cardiomyocyte proliferation decreases, and this increase is required for cardiomyocyte re-differentiation and successful long-term regeneration. Reduced upregulation of OXPHOS in Astyanax mexicanus cavefish results in the absence of a dynamic temporal sarcomere gene expression program during cardiomyocyte re-differentiation. These findings challenge the assumption that OXPHOS inhibits regeneration and reveal targetable pathways to enhance heart repair in humans after myocardial infarction.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s44161-025-00718-x

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Role:
Author
ORCID:
0000-0001-5044-2876
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Role:
Author
ORCID:
0000-0002-1632-6318
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Role:
Author
ORCID:
0000-0003-1889-3276
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Role:
Author
ORCID:
0000-0001-7618-9709


Publisher:
Springer Nature [academic journals on nature.com]
Journal:
Nature Cardiovascular Research More from this journal
Publication date:
2025-10-01
Acceptance date:
2025-08-26
DOI:
EISSN:
2731-0590
ISSN:
2731-0590


Language:
English
Pubs id:
2295937
Local pid:
pubs:2295937
Source identifiers:
W4414724579
Deposit date:
2025-10-03
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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