Phenotypic screening uncovered anti-myocardial fibrosis candidates using a novel 3D myocardial tissue under hypoxia.
10.1016/j.apsb.2025.04.025
- Author:
Jingyu WANG
1
;
Xiangning LIU
1
;
Rongxin ZHU
1
;
Ying SUN
1
;
Boyang JIAO
1
;
Keyan WANG
1
;
Yong JIANG
2
;
Yong WANG
3
;
Chun LI
4
;
Wei WANG
4
Author Information
1. School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China.
2. State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
3. Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100029, China.
4. Key Laboratory of Traditional Chinese Medicine Syndrome and Formula, Ministry of Education, Beijing 100029, China.
- Publication Type:Journal Article
- Keywords:
3D myocardial tissue;
Drug screening;
Hydrogel;
Hypoxia;
Myocardial fibrosis;
Primary cell;
Tissue contraction;
Toxicodendron vernicifluum
- From:
Acta Pharmaceutica Sinica B
2025;15(6):3008-3024
- CountryChina
- Language:English
-
Abstract:
Myocardial fibrosis (MF) is a common pathological hallmark of cardiovascular diseases, reflecting shared mechanisms in their progression. However, the lack of reliable MF models that accurately mimic its pathogenesis has hindered drug discovery, highlighting the urgent need for more effective therapeutic agents. Herein, a novel contractile three-dimensional (3D) myocardial tissue model integrating cardiomyocytes, cardiac-fibroblasts, and bone marrow-derived macrophages in collagen hydrogel was developed to simulate the fibrotic changes of cardiovascular disease, and facilitate the screening of anti-MF compounds. The 3D myocardial tissue model exhibited precise, visualizable, and quantifiable contractile characteristics under hypoxia and drug interventions. 76 compounds extracted from the resins of Toxicodendron vernicifluum, a traditional Chinese medicine with clear clinical benefits for fibrotic diseases, were screened for anti-fibrotic activity. Using an in vitro 3D oxygen-glucose deprivation (OGD)-treated myocardial tissue model instead of a two-dimensional transforming growth factor-β treated cardiac-fibroblasts model, two candidates including LQ-40 and SQ-3 exert impressive anti-MF activity, which was further validated in left anterior descending coronary artery ligation-induced MF mouse model. The current results demonstrate the feasibility and advantage of the novel contractile 3D tissue model with multi-cell types in discovering candidates for MF, further stressing the great potential of regulating macrophages in the treatment of MF.
