Department of Cardiology, Renmin Hospital of Wuhan University.
Cardiovascular Research Institute, Wuhan University.
Int Heart J. 2021 Mar 30;62(2):371-380. doi: 10.1536/ihj.20-016. Epub 2021 Mar 17.
Coronary artery disease (CAD) is one of the heavy health burdens worldwide. Aberrant proliferation of vascular smooth muscle cells (VSMCs) contributes to the occurrence and development of CAD. This study aimed at exploring differentially expressed microRNAs (miRNAs) and their regulatory mechanisms in the development of CAD.The miRNA expression profile of GSE28858 was obtained from the Gene Expression Omnibus database. Differentially expressed miRNAs (DEmiRNAs) between CAD and healthy control samples were analyzed using limma package in R. Target genes of DEmiRNAs were predicted, and a miRNA-target gene network was constructed. The relationship between miR-665 and transforming growth factor beta receptor 1 (TGFBR1) was selected for further analysis. The interaction between miR-665 and TGFBR1 was confirmed by dual luciferase reporter assay. Effects of miR-665 on cell viability and apoptosis of VSMCs were evaluated by cell counting kit-8 (CCK-8) assay and flow cytometry, respectively. Besides, western blot assays for BCL2L11 and caspase 3 were also conducted.A total of 38 upregulated miRNAs and 28 downregulated miRNAs were identified. The expression level of miR-665 was significantly downregulated in patients with CAD. TGFBR1 was proved to be a target gene of miR-665. Besides, ectopic expression of miR-665 obviously inhibited VSMC growth and promoted VSMC apoptosis. TGFBR1 overexpression in VSMCs transfected with miR-665 mimic could restore the effect of miR-665 on the proliferation and apoptosis of VSMCs.MiR-665 might participate in the proliferation and apoptosis of VSMCs by targeting TGFBR1.
冠状动脉疾病(CAD)是全球范围内的重大健康负担之一。血管平滑肌细胞(VSMCs)的异常增殖导致 CAD 的发生和发展。本研究旨在探索 CAD 发生发展过程中差异表达的 microRNAs(miRNAs)及其调控机制。从基因表达综合数据库中获取 GSE28858 的 miRNA 表达谱。使用 R 中的 limma 包分析 CAD 与健康对照样本之间的差异表达 miRNA(DEmiRNAs)。预测 DEmiRNAs 的靶基因,并构建 miRNA-靶基因网络。选择 miR-665 和转化生长因子β受体 1(TGFBR1)之间的关系进行进一步分析。通过双荧光素酶报告基因检测证实 miR-665 与 TGFBR1 的相互作用。通过细胞计数试剂盒-8(CCK-8)检测和流式细胞术分别评估 miR-665 对 VSMCs 活力和凋亡的影响。此外,还进行了 BCL2L11 和 caspase 3 的 Western blot 检测。鉴定出 38 个上调 miRNA 和 28 个下调 miRNA。CAD 患者 miR-665 的表达水平明显下调。TGFBR1 被证明是 miR-665 的靶基因。此外,外源性表达 miR-665 明显抑制 VSMC 生长并促进 VSMC 凋亡。在转染 miR-665 模拟物的 VSMCs 中转染 TGFBR1 过表达可以恢复 miR-665 对 VSMCs 增殖和凋亡的作用。miR-665 可能通过靶向 TGFBR1 参与 VSMCs 的增殖和凋亡。