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Stabilisation of HIF signalling in the mouse epicardium extends embryonic potential and neonatal heart regeneration

Abstract:
In humans, new-born infants can regenerate their heart during early life. This is modelled in the mouse, where regenerative capacity is maintained for the first week after birth but lost thereafter. Reactivation of this process holds great therapeutic potential; however, the molecular pathways that might be targeted to extend neonatal regeneration remain elusive. Here, we explored a role for hypoxia and HIF signalling on the regulation of epicardial activity in the developing mouse heart and in modulating the response to injury. Hypoxic regions were found in the epicardium from mid-gestation, associating with HIF-1α and HIF-2α, and expression of the epicardial master regulator Wilms’ tumour 1 (WT1). Epicardial deletion of Hif1α reduced WT1 levels, leading to impaired coronary vasculature. Targeting of the HIF degradation enzyme PHD, through pharmacological inhibition with a clinically approved drug or epicardial-specific genetic deletion of Egln1, stabilised HIF and promoted WT1 activity ex vivo. Finally, a combination of genetic and pharmacological stabilisation of HIF during neonatal heart injury led to prolonged epicardial activation, preservation of myocardium, augmented infarct resolution and preserved function beyond the 7-day regenerative window. These findings suggest modulation of HIF signalling extends epicardial activation to maintain myocardial survival beyond the neonatal regenerative window and may represent a viable strategy for treating ischaemic heart disease.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.7554/elife.107419

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Institution:
University of Oxford
Role:
Author
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Institution:
University of Oxford
Role:
Author
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Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Strategic
Role:
Author
ORCID:
0000-0001-8060-3706
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Institution:
University of Oxford
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Author
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Institution:
University of Oxford
Role:
Author


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Funder identifier:
https://ror.org/02wdwnk04


Publisher:
eLife Sciences Publications
Journal:
eLife More from this journal
Volume:
14
Article number:
RP107419
Publication date:
2025-10-22
DOI:
EISSN:
2050084X
ISSN:
2050084X


Language:
English
Keywords:
Source identifiers:
3398144
Deposit date:
2025-10-23
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