Department of Cardiology, The Second Clinic Medical College, Yangzhou University, Yangzhou, 225001, China.
Mol Biol Rep. 2012 Apr;39(4):4445-54. doi: 10.1007/s11033-011-1233-0. Epub 2011 Sep 25.
Circulating endothelial progenitor cells (EPCs) have a critical role in endothelial maintenance and repair. Apolipoprotein A-I mimetic peptide D-4F has been shown to posses anti-atherogenic properties via sequestration of oxidized phospholipids, induction of remodeling of high density lipoprotein and promotion of cholesterol efflux from macrophage-derived foam cells. In this study, we test the effects of D-4F on EPC biology. EPCs were isolated from the peripheral venous blood of healthy male volunteers and characterized by 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine-labeled acetylated LDL uptake and ulex europaeus agglutinin binding and flow cytometry. Cell proliferation, migration, adhesion, nitric oxide production and endothelial nitric oxide synthase (eNOS) expression in the absence and presence of D-4F or simvastatin (as a positive control), were assayed. We demonstrated that D-4F significantly enhanced EPC proliferation, migration and adhesion in a dose-dependent manner compared with vehicle. However, all of the favorable effects of D-4F on EPCs were dramatically attenuated by preincubation with NOS inhibitor L-NAME. Further, D-4F also increased nitric oxide production in culture supernatant and the levels of eNOS expression and phosphorylation. The stimulatory effects of D-4F (10 μg/ml) on EPC biology were comparable to 0.5 μM simvastatin. These results suggest that eNOS/NO pathway mediates the functional modulation of EPC biology in response to D-4F treatment and support the notion that the beneficial role of D-4F on EPCs may be one of the important components of its anti-atherogenic potential.
循环内皮祖细胞 (EPC) 在维持和修复内皮方面起着关键作用。载脂蛋白 A-I 模拟肽 D-4F 已被证明具有抗动脉粥样硬化特性,通过隔离氧化磷脂、诱导高密度脂蛋白重塑以及促进巨噬细胞源性泡沫细胞中的胆固醇流出。在这项研究中,我们测试了 D-4F 对 EPC 生物学的影响。EPC 从健康男性志愿者的外周静脉血中分离出来,并通过 1,1'-二辛基-3,3,3',3'-四甲基吲哚羰花青标记的乙酰化 LDL 摄取、欧洲菘蓝凝集素结合和流式细胞术进行表征。在不存在和存在 D-4F 或辛伐他汀(作为阳性对照)的情况下,测定细胞增殖、迁移、黏附、一氧化氮产生和内皮型一氧化氮合酶 (eNOS) 表达。与载体相比,我们证明 D-4F 以剂量依赖的方式显著增强 EPC 的增殖、迁移和黏附。然而,NOS 抑制剂 L-NAME 预先孵育显著减弱了 D-4F 对 EPC 的所有有利作用。此外,D-4F 还增加了培养上清液中一氧化氮的产生以及 eNOS 表达和磷酸化水平。D-4F(10μg/ml)对 EPC 生物学的刺激作用与 0.5μM 辛伐他汀相当。这些结果表明,eNOS/NO 途径介导了 D-4F 处理对 EPC 生物学功能的调节,并支持 D-4F 对 EPC 的有益作用可能是其抗动脉粥样硬化潜力的重要组成部分之一的观点。