微小RNA-125a-5p部分调节氧化型低密度脂蛋白刺激的单核细胞/巨噬细胞中的炎症反应、脂质摄取和氧化还原蛋白9(ORP9)表达。
MicroRNA-125a-5p partly regulates the inflammatory response, lipid uptake, and ORP9 expression in oxLDL-stimulated monocyte/macrophages.
作者信息
Chen Ting, Huang Zhouqing, Wang Liansheng, Wang Yue, Wu Feizhen, Meng Shu, Wang Changqian
机构信息
Department of Cardiology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, 1665 Kongjiang Road, Shanghai, Peoples Republic of China.
出版信息
Cardiovasc Res. 2009 Jul 1;83(1):131-9. doi: 10.1093/cvr/cvp121. Epub 2009 Apr 17.
AIMS
The inflammatory responses of monocytes/macrophages and the stimulation of lipid uptake into these cells by oxidized low density lipoprotein (oxLDL) are critical to the initiation and development of atherosclerosis. Increasing evidence has demonstrated that many microRNAs play important roles in the cell proliferation, apoptosis, and differentiation that accompany inflammatory responses. However, whether microRNAs are associated with monocyte/macrophage inflammatory responses or oxLDL stimulation is not yet known. The aim of the present study is to investigate microRNAs in monocytes/macrophages and their potential role in oxLDL-stimulation of lipid uptake and other atherosclerotic responses.
METHODS AND RESULTS
Microarrays were used to analyse the global expression of microRNAs in oxLDL-stimulated human primary peripheral blood monocytes. Expression profiles of the microRNAs were verified using TaqMan real-time PCR. Five microRNAs (microRNA-125a-5p, microRNA-9, microRNA-146a, microRNA-146b-5p, and microRNA-155) were aberrantly expressed after oxLDL treatment of human primary monocytes. Bioinformatics analysis suggested that microRNA-125a-5p is related to a protein similar to ORP9 (oxysterol binding protein-like 9) and this was confirmed by a luciferase reporter assay. MicroRNA-125a-5p was found to mediate lipid uptake and to decrease the secretion of some inflammatory cytokines (interleukin-2, interleukin-6, tumour necrosis factor-alpha, transforming growth factor-beta) in oxLDL-stimulated monocyte-derived macrophages.
CONCLUSION
MicroRNA-125a-5p may partly provide post-transcriptional regulation of the proinflammatory response, lipid uptake, and expression of ORP9 in oxLDL-stimulated monocyte/macrophages.
目的
单核细胞/巨噬细胞的炎症反应以及氧化型低密度脂蛋白(oxLDL)对这些细胞脂质摄取的刺激作用,对动脉粥样硬化的发生和发展至关重要。越来越多的证据表明,许多微小RNA在伴随炎症反应的细胞增殖、凋亡和分化过程中发挥重要作用。然而,微小RNA是否与单核细胞/巨噬细胞的炎症反应或oxLDL刺激相关尚不清楚。本研究的目的是调查单核细胞/巨噬细胞中的微小RNA及其在oxLDL刺激脂质摄取和其他动脉粥样硬化反应中的潜在作用。
方法与结果
使用微阵列分析oxLDL刺激的人原代外周血单核细胞中微小RNA的整体表达情况。通过TaqMan实时PCR验证微小RNA的表达谱。在oxLDL处理人原代单核细胞后,有5种微小RNA(微小RNA-125a-5p、微小RNA-9、微小RNA-146a、微小RNA-146b-5p和微小RNA-155)表达异常。生物信息学分析表明,微小RNA-125a-5p与一种类似于ORP9(氧化固醇结合蛋白样9)的蛋白质相关,荧光素酶报告基因检测证实了这一点。研究发现,微小RNA-125a-5p在oxLDL刺激的单核细胞衍生巨噬细胞中介导脂质摄取,并减少一些炎性细胞因子(白细胞介素-2、白细胞介素-6、肿瘤坏死因子-α、转化生长因子-β)的分泌。
结论
微小RNA-125a-5p可能部分提供对oxLDL刺激的单核细胞/巨噬细胞中促炎反应、脂质摄取和ORP9表达的转录后调控。