A zebrafish model of chronic heart failure caused by protein aggregation in heart valves

We previously developed a unique zebrafish, tomato, expressing the red fluorescent protein DsRed under the control of the tph2 promoter. Unexpectedly, the tomato fish showed cardiac dilation and symptoms resembling those of chronic heart failure. Therefore, we investigate the pathogenesis and causes of these cardiac abnormalities. Crossbreeding suggests a link between DsRed expression and heart enlargement. Histological analysis confirms atrial dilation and thickening of the atrioventricular valve. RNA sequencing and immunohistological imaging reveal that valve thickness is due to the upregulated inflammation, cell proliferation, and epithelial-mesenchymal transition. Importantly, immunohistological staining elucidates DsRed accumulation in the atrioventricular valve, and removal of DsRed via Cre-mRNA injection rescues these heart defects. This study establishes a potential model of heart failure caused by protein aggregation in the cardiac valve. These findings highlight the potential of this transgenic zebrafish for investigating valvular heart diseases and chronic heart failure and developing new therapies.

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Publication Details

Journal
Communications Biology
Published
2025-11-04
DOI
https://doi.org/10.1038/s42003-025-08882-3
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
0.00

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article

A zebrafish model of chronic heart failure caused by protein aggregation in heart valves

Ryo Kimura, Yitong Li, Shu Suzuki, S. Maegawa et al.
Communications Biology
Congenital heart defects research
article

A zebrafish model of chronic heart failure caused by protein aggregation in heart valves

Ryo Kimura, Yitong Li, Shu Suzuki, S. Maegawa, Taiki Nishimura
article en

Abstract

We previously developed a unique zebrafish, tomato, expressing the red fluorescent protein DsRed under the control of the tph2 promoter. Unexpectedly, the tomato fish showed cardiac dilation and symptoms resembling those of chronic heart failure. Therefore, we investigate the pathogenesis and causes of these cardiac abnormalities. Crossbreeding suggests a link between DsRed expression and heart enlargement. Histological analysis confirms atrial dilation and thickening of the atrioventricular valve. RNA sequencing and immunohistological imaging reveal that valve thickness is due to the upregulated inflammation, cell proliferation, and epithelial-mesenchymal transition. Importantly, immunohistological staining elucidates DsRed accumulation in the atrioventricular valve, and removal of DsRed via Cre-mRNA injection rescues these heart defects. This study establishes a potential model of heart failure caused by protein aggregation in the cardiac valve. These findings highlight the potential of this transgenic zebrafish for investigating valvular heart diseases and chronic heart failure and developing new therapies.

Communications BiologyVol. 8(1)
Kyoto University (JP), Child Development Center (QA), The University of Osaka (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 71%
Congenital heart defects research
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A zebrafish model of chronic heart failure caused by protein aggregation in heart valves — Ryo Kimura, Yitong Li, et al. · Communications Biology (2025) | TGRS Research Map | TGRS