Inhibition of activin A receptor signalling attenuates age-related pathological cardiac remodelling

[thumbnail of Open Access]
Preview
Text (Open Access) - Published Version
· Available under License Creative Commons Attribution.
· Please see our End User Agreement before downloading.
| Preview
Available under license: Creative Commons Attribution

Please see our End User Agreement.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

Add to AnyAdd to TwitterAdd to FacebookAdd to LinkedinAdd to PinterestAdd to Email

Clavere, N. G., Alqallaf, A., Rostron, K. A., Parnell, A., Mitchell, R., Patel, K. and Boateng, S. Y. (2022) Inhibition of activin A receptor signalling attenuates age-related pathological cardiac remodelling. Disease Models & Mechanisms, 15 (5). dmm049424. ISSN 1754-8411 doi: 10.1242/dmm.049424

Abstract/Summary

In the heart, ageing is associated with DNA damage, oxidative stress, fibrosis and activation of the activin signalling pathway, leading to cardiac dysfunction. The cardiac effects of activin signalling blockade in progeria are unknown. This study investigated the cardiac effects of progeria induced by attenuated levels of Ercc1 required for DNA excision/repair and the impact of activin signalling blockade using a soluble activin receptor type IIB (sActRIIB). DNA damage and oxidative stress were significantly increased in Ercc1Δ/- hearts but were reduced by sActRIIB treatment. sActRIIB treatment improved cardiac systolic function and induced cardiomyocyte hypertrophy in Ercc1Δ/- hearts. RNA-seq analysis showed that in Ercc1Δ/- hearts there was an increase in pro-oxidant and a decrease in antioxidant gene expression, whilst sActRIIB treatment reversed this. Ercc1Δ/- hearts also expressed higher levels of anti-hypertrophic genes and a decrease in pro-hypertrophic ones which were also reversed by sActRIIB treatment. These results show for the first time that inhibition of activin A receptor signalling attenuates cardiac dysfunction, pathological tissue remodelling and gene expression in Ercc1 deficient mice and presents a potentially novel therapeutic target for heart diseases.

Altmetric Badge

Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/105485
Identification Number/DOI 10.1242/dmm.049424
Refereed Yes
Divisions Life Sciences > School of Biological Sciences > Biomedical Sciences
Publisher The Company of Biologists
Download/View statistics View download statistics for this item

Downloads

Downloads per month over past year

University Staff: Request a correction | Centaur Editors: Update this record

Search Google Scholar