Yang G, Zhang Z, Ma X, Chen J, Shi H, Yang J, Han Q
The First School of Clinical Medicine, Shanxi Medical University, Taiyuan, China,
Physiol Res. 2025 Aug 31;74(4):577-588. doi: 10.33549/physiolres.935564.
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.
血管平滑肌细胞(VSMC)的增殖和迁移是接受经皮冠状动脉介入治疗(PCI)患者再狭窄的初始促成因素。微小RNA - 145(miR - 145)在这一病理过程中发挥重要作用。虽然已证明卡维地洛可抑制VSMC增殖和迁移,但其潜在机制尚未完全明确。我们研究的目的是检验卡维地洛是否调节miR - 145的表达,从而抑制VSMC的增殖和迁移能力。培养VSMC并用miR - 145模拟物或miR - 145抑制剂进行转染。使用细胞计数试剂盒 - 8(CCK - 8)和5 - 乙炔基 - 2'-脱氧尿苷(EdU)试验评估细胞增殖,同时使用伤口愈合试验和Transwell试验评估迁移能力。使用蛋白质印迹分析对蛋白质表达水平进行定量,此外,进行荧光素酶报告基因试验以鉴定miR - 145的靶基因。我们发现卡维地洛上调miR - 145的表达并降低Krüppel样因子4(KLF4)的表达。此外,miR - 145抑制VSMC增殖和迁移。KLF4被鉴定为miR - 145的直接靶标。重要的是,抑制miR - 145减弱了卡维地洛对VSMC的抑制作用。总之,我们的研究结果表明,卡维地洛至少部分通过上调miR - 145对VSMC增殖和迁移发挥抑制作用。这些发现表明,miR - 145可能是卡维地洛对VSMC治疗作用的关键介质。