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Isolation of Primary Patient-specific Aortic Smooth Muscle Cells and Semiquantitative Real-time Contraction Measurements In Vitro
Published on: February 15, 2022
Hsa_circ_0032389 Enhances Proliferation and Migration in PDGF-BB-Induced Human Aortic Vascular Smooth Muscle Cells
Haiyun Qian1, Shengwei Ma2, Qian Zhou2
1Surgical Department of Cardiothoracic Macrovascular, Jingzhou Hospital Affiliated to Yangtze University, No.26 Chuyuan Avenue, Jingzhou District, Jingzhou, 434020, Hubei, China. qianhaiyun@yangtzeu.edu.cn.
Circular RNA hsa_circ_0032389 promotes atherosclerosis by enhancing vascular smooth muscle cell proliferation and migration. It acts as a sponge for miR-513a-5p, which targets FRS2, thus driving disease progression.
Area of Science:
- Cardiovascular Biology
- Molecular Biology
- RNA Biology
Background:
- Circular RNAs (circRNAs) are implicated in atherosclerosis (AS) pathogenesis.
- The specific role of hsa_circ_0032389 in AS requires elucidation.
Purpose of the Study:
- To investigate the function and mechanism of hsa_circ_0032389 in AS.
- To explore its regulation of human aortic vascular smooth muscle cells (HA-VSMCs) under platelet-derived growth factor-BB (PDGF-BB) stimulation.
Main Methods:
- Quantitative real-time PCR to measure gene expression.
- Cell proliferation and migration assays (CCK-8, flow cytometry, EdU, Transwell, wound healing).
- Western blot, dual-luciferase reporter, and RIP assays to confirm molecular interactions.
Main Results:
- Hsa_circ_0032389 was upregulated in PDGF-BB-induced HA-VSMCs.
- Downregulation of hsa_circ_0032389 inhibited HA-VSMC proliferation and migration.
- Hsa_circ_0032389 sponged miR-513a-5p, and miR-513a-5p targeted FRS2.
- The miR-513a-5p/FRS2 axis mediated the effects of hsa_circ_0032389.
Conclusions:
- Hsa_circ_0032389 promotes PDGF-BB-induced HA-VSMC proliferation and migration.
- This occurs via the hsa_circ_0032389/miR-513a-5p/FRS2 regulatory pathway.
- Hsa_circ_0032389 is a potential therapeutic target for atherosclerosis.
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