Related Experiment Video
Updated: Sep 9, 2025

Isolation of Primary Patient-specific Aortic Smooth Muscle Cells and Semiquantitative Real-time Contraction Measurements In Vitro
Published on: February 15, 2022
Role of Carvedilol in Inhibiting the Proliferation and Migration of Vascular Smooth Muscle Cells by Upregulating
1The First School of Clinical Medicine, Shanxi Medical University, Taiyuan, China, qinghuahanhqh@126.com.
Abstract:
The proliferation and migration of vascular smooth muscle cells (VSMCs) are the initial contributors to restenosis in patients undergoing percutaneous coronary intervention (PCI). MicroRNA-145 (miR-145) plays a significant role in this pathological process. Although carvedilol has been shown to inhibit VSMC proliferation and migration, the underlying mechanisms are not fully understood. The aim of our study is to examine whether carvedilol regulates the expression of miR-145 and thereby inhibits the proliferation and migrative capacity of VSMCs. VSMCs were cultured and transfected with either miR-145 mimics or miR-145 inhibitors. Cell proliferation was evaluated using the Cell Counting Kit-8 (CCK-8) and 5-ethynyl-2?-deoxyuridine (EdU) assays, while wound healing and Transwell assays were used to assess the migration capacity. Protein expression levels were quantified using western blot analysis, and additionally, a luciferase reporter assay was performed to identify the target gene of miR-145. We found that carvedilol upregulated the expression of miR-145 and decreased the expression of Krüppel-like factor 4 (KLF4). Furthermore, miR-145 inhibited VSMC proliferation and migration. KLF4 was identified as a direct target of miR-145. Importantly, the inhibition of miR-145 attenuated the suppressive effects of carvedilol on VSMCs. In summary, our results in this study demonstrate that carvedilol exerts its inhibitory effects on VSMC proliferation and migration, at least in part, through the upregulation of miR-145. These findings suggest that miR-145 may be a key mediator in the therapeutic effects of carvedilol on VSMCs.
Insights
Carvedilol inhibits vascular smooth muscle cell proliferation and migration by increasing microRNA-145 (miR-145) levels. This study reveals miR-145 as a key mediator in carvedilol
Area of Science:
- Cardiovascular Biology
- Molecular Medicine
- Cell Biology
Background:
- Vascular smooth muscle cell (VSMC) proliferation and migration are key drivers of restenosis after percutaneous coronary intervention (PCI).
- MicroRNA-145 (miR-145) is implicated in VSMC pathobiology.
- The precise mechanism by which carvedilol inhibits VSMC activity remains incompletely understood.
Purpose of the Study:
- To investigate if carvedilol modulates miR-145 expression.
- To determine if miR-145 mediates carvedilol's inhibitory effects on VSMC proliferation and migration.
Main Methods:
- VSMCs were treated with miR-145 mimics or inhibitors.
- Cell proliferation was assessed using CCK-8 and EdU assays.
- Cell migration was evaluated via wound healing and Transwell assays.
- Protein expression and miR-145 targets were analyzed using Western blot and luciferase reporter assays.
Main Results:
- Carvedilol treatment upregulated miR-145 expression and downregulated Krüppel-like factor 4 (KLF4).
- Overexpression of miR-145 inhibited VSMC proliferation and migration.
- KLF4 was confirmed as a direct target of miR-145.
- Inhibition of miR-145 diminished the anti-proliferative and anti-migratory effects of carvedilol.
Conclusions:
- Carvedilol inhibits VSMC proliferation and migration, partly by upregulating miR-145.
- miR-145 acts as a crucial mediator in the therapeutic action of carvedilol on VSMCs.
- These findings highlight miR-145 as a potential therapeutic target for preventing restenosis.
Related Concept Videos
Antihypertensive Drugs: Vasodilators
Antihypertensive Drugs: Action of Calcium Channel Blockers
Adrenergic Antagonists: ɑ and β-Receptor Blockers
Regulation of Angiogenesis and Blood Supply
Heart Failure Drugs: β-Blockers
Antianginal Drugs: Calcium Channel Blockers and Ranolazine
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...

