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2
Ginkgo biloba extract inhibits oxidized low-density lipoprotein (oxLDL)-induced matrix metalloproteinase activation by the modulation of the lectin-like oxLDL receptor 1-regulated signaling pathway in human umbilical vein endothelial cells.银杏叶提取物通过调节人脐静脉内皮细胞中凝集素样氧化低密度脂蛋白受体1调控的信号通路,抑制氧化低密度脂蛋白(oxLDL)诱导的基质金属蛋白酶激活。
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3
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本文引用的文献

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Influenza virus aggravates the ox-LDL-induced apoptosis of human endothelial cells via promoting p53 signaling.流感病毒通过促进 p53 信号通路加重 ox-LDL 诱导的人内皮细胞凋亡。
J Med Virol. 2015 Jul;87(7):1113-23. doi: 10.1002/jmv.24166. Epub 2015 Mar 16.
2
Oxidized low-density lipoprotein induces long-term proinflammatory cytokine production and foam cell formation via epigenetic reprogramming of monocytes.氧化型低密度脂蛋白通过单核细胞的表观遗传重编程诱导长期促炎细胞因子产生和泡沫细胞形成。
Arterioscler Thromb Vasc Biol. 2014 Aug;34(8):1731-8. doi: 10.1161/ATVBAHA.114.303887. Epub 2014 Jun 5.
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Matrix metalloproteinase (MMP)-9: a proximal biomarker for cardiac remodeling and a distal biomarker for inflammation.基质金属蛋白酶(MMP)-9:心脏重构的近端生物标志物和炎症的远端生物标志物。
Pharmacol Ther. 2013 Jul;139(1):32-40. doi: 10.1016/j.pharmthera.2013.03.009. Epub 2013 Apr 3.
4
Oxidized low-density lipoprotein as a biomarker of in vivo oxidative stress: from atherosclerosis to periodontitis.氧化型低密度脂蛋白作为体内氧化应激的生物标志物:从动脉粥样硬化到牙周炎。
J Clin Biochem Nutr. 2012 Jul;51(1):1-8. doi: 10.3164/jcbn.11-00020R1. Epub 2012 Mar 30.
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Infections may be causal in the pathogenesis of atherosclerosis.感染可能是动脉粥样硬化发病机制中的一个因果因素。
Am J Med Sci. 2012 Nov;344(5):391-4. doi: 10.1097/MAJ.0b013e31824ba6e0.
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Herpes simplex virus type 2 (HSV-2) as a coronary atherosclerosis risk factor in HIV-infected men: multicenter AIDS cohort study.单纯疱疹病毒 2 型(HSV-2)作为感染 HIV 的男性冠心病的一个危险因素:多中心艾滋病队列研究。
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Influenza virus directly infects, inflames, and resides in the arteries of atherosclerotic and normal mice.流感病毒直接感染、炎症反应并寄居在动脉粥样硬化和正常小鼠的动脉中。
Atherosclerosis. 2010 Jan;208(1):90-6. doi: 10.1016/j.atherosclerosis.2009.07.028. Epub 2009 Jul 24.
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Proinflammatory and prothrombotic effects on human vascular endothelial cells of immune-cell-derived LIGHT.免疫细胞衍生的LIGHT对人血管内皮细胞的促炎和促血栓形成作用。
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Circulating oxidized low-density lipoprotein: a biomarker of atherosclerosis and cardiovascular risk?循环氧化低密度脂蛋白:动脉粥样硬化和心血管风险的生物标志物?
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10
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流感病毒感染和氧化低密度脂蛋白处理对人内皮细胞基质金属蛋白酶-9表达及促炎细胞因子的协同增强作用

Synergistic enhancement of matrix metalloproteinase-9 expression and pro-inflammatory cytokines by influenza virus infection and oxidized-LDL treatment in human endothelial cells.

作者信息

Wu Yun, Huang He

机构信息

Department of Cardiovascular Medicine, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China.

Cardiovascular Research Institute, Wuhan University, Wuhan, Hubei 430060, P.R. China.

出版信息

Exp Ther Med. 2017 Nov;14(5):4579-4585. doi: 10.3892/etm.2017.5099. Epub 2017 Sep 1.

DOI:10.3892/etm.2017.5099
PMID:29104665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5658766/
Abstract

Oxidized low-density lipoprotein (oxLDL) has been reported to contribute to the development and progression of atherosclerosis, which is also stimulated by viral infections, such as influenza. However, the mechanism underlining the promotion of atherosclerosis by both risk factors remains unclear. In the present study, we investigated the expression of matrix metalloproteinase-9 (MMP-9), which is one of key mediators of atherosclerosis progression, in oxLDL-treated human umbilical vein endothelial cells (HUVEC)-C cells. The infection efficiency of H1N1 pdm2009 influenza virus in the HUVEC-C cells was subsequently examined, and the expression of MMP-9 and proinflammatory cytokines, including tumor necrosis factor (TNF)-α, interleukin (IL)-1β and IL-6, were determined in the virus-infected HUVEC-C cells, with or without oxLDL treatment. Results demonstrated that oxLDL treatment with 10, 20 or 50 µg/ml markedly upregulated MMP-9 expression at the mRNA and protein levels. H1N1 pdm2009 influenza virus efficiently infected the HUVEC-C cells and significantly promoted the expression of MMP-9, TNF-α, IL-1β and IL-6, synergistically with the oxLDL treatment. Taken together, these results demonstrated for the first time that oxidized-LDL treatment and influenza virus infection synergistically enhance the expression of MMP-9 and proinflammatory cytokines in human endothelial cells, suggesting that both factors are potent stimulators in atherosclerotic impairment to endothelial cells.

摘要

据报道,氧化型低密度脂蛋白(oxLDL)会促进动脉粥样硬化的发生和发展,而病毒感染(如流感)也会刺激动脉粥样硬化。然而,这两种危险因素促进动脉粥样硬化的潜在机制仍不清楚。在本研究中,我们调查了基质金属蛋白酶-9(MMP-9)的表达,MMP-9是动脉粥样硬化进展的关键介质之一,在oxLDL处理的人脐静脉内皮细胞(HUVEC-C)中。随后检测了2009年甲型H1N1流感病毒在HUVEC-C细胞中的感染效率,并测定了在有或没有oxLDL处理的病毒感染的HUVEC-C细胞中MMP-9和促炎细胞因子的表达,包括肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β和IL-6。结果表明,10、20或50μg/ml的oxLDL处理在mRNA和蛋白质水平上显著上调了MMP-9的表达。2009年甲型H1N1流感病毒有效地感染了HUVEC-C细胞,并与oxLDL处理协同显著促进了MMP-9、TNF-α、IL-1β和IL-6的表达。综上所述,这些结果首次证明氧化型LDL处理和流感病毒感染协同增强了人内皮细胞中MMP-9和促炎细胞因子的表达,表明这两种因素都是动脉粥样硬化损伤内皮细胞的有效刺激物。