Adipocyte enhancer binding protein 1 (AEBP1) inhibition mediates cardiac reverse remodeling by regulating MRTFB and RUNX2 signaling

Abstract Persistent activation of fibroblasts to myofibroblasts leads to increased myocardial fibrosis which is often detrimental to cardiac function and leads to heart failure (HF). Adipocyte enhancer binding protein (AEBP1) plays a crucial role in fibroblast activation following injury in the kidney, liver, and lungs. AEBP1 inhibition resulted in fibrosis attenuation in these organs. AEBP1 has been reported to be upregulated in the HF myocardium, however, its role in cardiac fibrosis progression is not well understood. In this study, we show that AEBP1 is crucial for cardiac fibroblast activation and AEBP1 inhibition prevents cardiac fibroblast differentiation in vitro. AEBP1 knock-down (KD) in mouse models of acute cardiac fibrosis improved cardiac structure and function. Tissue culture studies of non-failing donor myocardium resulted in increased cellular hypertrophy and tissue remodeling following AEBP1 overexpression. Contrarily, a significant improvement in cardiac structure evident from reduced cardiomyocyte hypertrophy and reduced fibrosis was observed in chronic HF myocardium following AEBP1 KD. Overall, we show that AEBP1 plays a critical role in fibrogenesis, and its inhibition has the potential to attenuate fibrosis in acute and chronic HF.

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Publication Details

Journal
Nature Communications
Published
2026-11-06
DOI
https://doi.org/10.1038/s41467-026-79136-x
Citations
1
Primary Topic
Cardiac Fibrosis and Remodeling
Type
article
Field-Weighted Citation Impact
4.00

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article

Adipocyte enhancer binding protein 1 (AEBP1) inhibition mediates cardiac reverse remodeling by regulating MRTFB and RUNX2 signaling

Junedh Amrute, Joseph R. Visker, Kory J. Lavine, Thomas Seidel et al.
1 citations
Nature Communications
Cardiac Fibrosis and Remodeling
4.00
article

Adipocyte enhancer binding protein 1 (AEBP1) inhibition mediates cardiac reverse remodeling by regulating MRTFB and RUNX2 signaling

Junedh Amrute, Joseph R. Visker, Kory J. Lavine, Thomas Seidel, Dipayan Chaudhuri, James Jeong, Ty Lunde, Dallen Calder, Konstantinos Sideris, Stavros George Drakos, Sutip Navankasattusas, Sihem Boudina, Rana Hamouche, Matthew D. Layne, Frank B. Sachse, Thirupura Sundari Shankar, Georgiy Polishchuk, Eleni Tseliou, Harini Srinivasan, Jing Ling, Craig Selzman, Ezra Johnson, Laisha padilla, Ioannis Kyriakoulis, Bassel Tekarli
article en
1 citations

Abstract

Abstract Persistent activation of fibroblasts to myofibroblasts leads to increased myocardial fibrosis which is often detrimental to cardiac function and leads to heart failure (HF). Adipocyte enhancer binding protein (AEBP1) plays a crucial role in fibroblast activation following injury in the kidney, liver, and lungs. AEBP1 inhibition resulted in fibrosis attenuation in these organs. AEBP1 has been reported to be upregulated in the HF myocardium, however, its role in cardiac fibrosis progression is not well understood. In this study, we show that AEBP1 is crucial for cardiac fibroblast activation and AEBP1 inhibition prevents cardiac fibroblast differentiation in vitro. AEBP1 knock-down (KD) in mouse models of acute cardiac fibrosis improved cardiac structure and function. Tissue culture studies of non-failing donor myocardium resulted in increased cellular hypertrophy and tissue remodeling following AEBP1 overexpression. Contrarily, a significant improvement in cardiac structure evident from reduced cardiomyocyte hypertrophy and reduced fibrosis was observed in chronic HF myocardium following AEBP1 KD. Overall, we show that AEBP1 plays a critical role in fibrogenesis, and its inhibition has the potential to attenuate fibrosis in acute and chronic HF.

Nature Communications
Boston University (US), Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), Washington University in St. Louis (US), University of Utah (US), University of Utah Health Care (US)
U.S. Department of Veterans Affairs, American Heart Association, Huntsman Cancer Institute, National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases
Good health and well-being
Openalex Percentile: Top 12%
Cardiac Fibrosis and Remodeling
4.00
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