Yang Jing, Zhou Xiaoman, Lu Jingwei, Li Meng
Department of Cardiology, The Fourth Hospital of Harbin Medical University, Harbin 150001, Heilongjiang, China.
Department of Radiology, Wuhan Pulmonary Hospital, Wuhan 430030, Hubei, China.
Open Med (Wars). 2022 Sep 24;17(1):1515-1527. doi: 10.1515/med-2022-0471. eCollection 2022.
Vascular calcification is a prominent manifestation of advanced atherosclerosis. Tumor necrosis factor-receptor-associated factors (TRAFs) were reported to participate in atherosclerosis development. In this study, the role and mechanism of TRAF6 in vascular calcification were explored. To induce the vascular calcification, oxidized low-density lipoprotein (Ox-LDL) was applied to treat vascular smooth muscle cells (VSMCs). TRAF6 protein expression in VSMCs was assessed by western blotting. Osteogenic differentiation of VSMCs was assessed by alkaline phosphatase activity analysis. Mineral deposition in VSMCs was evaluated by von Kossa staining. VSMC proliferation, migration, apoptosis, inflammation, and reactive oxygen species (ROS) generation were detected using cell counting kit-8, Transwell, flow cytometry, reverse transcriptase quantitative polymerase chain reaction (RT-qPCR), and dichlorodihydrofluorescein diacetate staining, respectively. Luciferase reporter assay was utilized to identify the binding relationship between miR-146-5p and TRAF6 in VSMCs. We found that Ox-LDL administration induced the calcification of VSMCs and elevated the TRAF6 level. TRAF6 knockdown restrained VSMC calcification, proliferation, migration, inflammation, and ROS generation caused by Ox-LDL. Mechanically, TRAF6 was targeted by miR-146-5p in VSMCs. Furthermore, TRAF6 overexpression offset the inhibitory effects of miR-146-5p upregulation on vascular calcification in VSMCs under the Ox-LDL condition. Overall, miR-146-5p restrains the calcification of VSMCs by suppressing TRAF6.
血管钙化是晚期动脉粥样硬化的一个显著表现。据报道,肿瘤坏死因子受体相关因子(TRAFs)参与动脉粥样硬化的发展。在本研究中,探讨了TRAF6在血管钙化中的作用及机制。为诱导血管钙化,应用氧化低密度脂蛋白(Ox-LDL)处理血管平滑肌细胞(VSMCs)。通过蛋白质免疫印迹法评估VSMCs中TRAF6蛋白的表达。通过碱性磷酸酶活性分析评估VSMCs的成骨分化。通过冯库萨染色评估VSMCs中的矿物质沉积。分别使用细胞计数试剂盒-8、Transwell、流式细胞术、逆转录定量聚合酶链反应(RT-qPCR)和二氯二氢荧光素二乙酸酯染色检测VSMC的增殖、迁移、凋亡、炎症和活性氧(ROS)生成。利用荧光素酶报告基因检测法确定miR-146-5p与VSMCs中TRAF6的结合关系。我们发现给予Ox-LDL可诱导VSMCs钙化并提高TRAF6水平。敲低TRAF6可抑制Ox-LDL引起的VSMC钙化、增殖、迁移、炎症和ROS生成。机制上,miR-146-5p在VSMCs中靶向作用于TRAF6。此外,在Ox-LDL条件下,TRAF6过表达抵消了miR-146-5p上调对VSMCs血管钙化的抑制作用。总体而言,miR-146-5p通过抑制TRAF6来抑制VSMCs的钙化。