The ADP-ribosyltransferases 3 (ART3) is a novel suppressor of pathological cardiac hypertrophy by ribosylating ITGA7
Pathological cardiac hypertrophy and heart failure remain mechanistically incompletely defined despite their clinical significance in cardiovascular disease. While ADP-ribosyltransferase cholera toxin-like (ARTC) enzymes modulate membrane protein function and downstream signaling via post-translational modifications, their role in cardiac pathology remains unexplored. Herein, we investigated the regulatory involvement of ADP-ribosyltransferase 3 (ART3) in myocardial remodeling. Cardiomyocyte-specific ART3 knockdown and overexpression murine models were established using adeno-associated virus serotype 9 (AAV9), with RNA-sequencing employed to profile ART3-dependent transcriptional responses in pathological cardiac hypertrophy. Functional validation was performed in complementary in vitro and in vivo hypertrophy models, complemented by immunoprecipitation-coupled mass spectrometry to identify ART3 substrates. ART3 was found to be cardiomyocyte-enriched and transcriptionally downregulated during progressive myocardial remodeling and heart failure. Cardiomyocyte-specific ART3 knockdown 3 accelerated the decompensatory transition of cardiac hypertrophy, whereas ART3 overexpression exerted significant anti-hypertrophic and anti-remodeling effects. Mechanistically, ART3 preserved cardiomyocyte mono-ADP-ribosyltransferase activity, catalyzing the site-specific mono-ADP-ribosylation (mADPr) of Integrin Subunit Alpha 7 (ITGA7) at residue R129. This post-translational modification was requisite for integrin signaling pathway activation, which mediated the observed cardioprotective effects. Collectively, these findings establish ART3 as a novel regulator of pathological cardiac hypertrophy by modulating ITGA7 via mADPr, highlighting its therapeutic potential as a target for heart failure intervention.
Authors
- Xiao Tao (ORCID: https://orcid.org/0000-0002-9381-7903)
- Agapios Sachinidis (ORCID: https://orcid.org/0000-0003-3054-225X)
- Luying Peng (ORCID: https://orcid.org/0000-0002-0033-767X)
- Li Li (ORCID: https://orcid.org/0009-0003-4636-9487)
- Yongfu Xiong (ORCID: https://orcid.org/0000-0001-9016-8509)
- Fang Lin
- Hanrui Wang
- Na Yi
- Qin Lin
- Yilei Meng
- Cuimei Zhao
- Haojie Lu
- Jie Sheng
- Yuping Zhu
- Ye Xu
- Mingxing Lu
- Chenyu Li
- Yizhuo Sun
- Sangyu Hu
Institutions
- Tongji University (CN)
- University of Cologne (DE)
- Fudan University (CN)
- Shanghai East Hospital (CN)
- Tongji Hospital (CN)
Publication Details
- Journal
- Acta Pharmaceutica Sinica B
- Published
- 2026-07-01
- DOI
- https://doi.org/10.1016/j.apsb.2026.06.053
- Primary Topic
- PARP inhibition in cancer therapy
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Science and Technology Commission of Shanghai Municipality