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Oleacein and Foam Cell Formation in Human Monocyte-Derived Macrophages: A Potential Strategy against Early and Advanced Atherosclerotic Lesions

机译:人单核细胞衍生的巨噬细胞中的糖素和泡沫细胞形成:针对早期和晚期动脉粥样硬化病变的潜在策略

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摘要

Background: Oleacein is a secoiridoid group polyphenol found mostly in L. and L. (Oleaceae). The aim of the present study was to investigate a potential role of oleacein in prevention of the foam cell formation. Materials and Methods: Oleacein was isolated from leaves. Human monocyte-derived macrophages were obtained from monocytes cultured with Granulocyte-macrophage colony-stimulating factor (GM-CSF). Then, cells were incubated with 20 μM or 50 μM of oleacein and with oxidized low-density lipoprotein (oxLDL) (50 μg/mL). Visualization of lipid deposition within macrophages was carried out using Oil-Red-O. Expression of CD36, Scavenger receptor A1 (SRA1) and Lectin-like oxidized low-density lipoprotein receptor 1 (LOX-1) was determined by Reverse transcription polymerase chain reaction (RT-PCR) and by flow cytometry. Apoptosis was determined by flow cytometry using Annexin V assay. STAT3 and Acyl-coenzyme A: cholesterol acyltransferase type 1 (ACAT1) levels were determined by ELISA. P-STAT3, P-JAK1, P-JAK2 expressions were determined by Western blot (WB). Results: Oleacein in dose-dependent manner significantly reduced lipid deposits in macrophages as well as their expression of selected scavenger receptors. The highest decrease of expression was found for CD36 and SRA1 receptors, from above 20% to more than 75% compared to oxLDL and the lowest for LOX-1 receptor, from approx. 8% to approx. 25% compared to oxLDL-stimulated macrophages. Oleacein significantly reduced (2.5-fold) early apoptosis of oxLDL-stimulated macrophages. Moreover, oleacein significantly increased the protein expression of JAK/STAT3 pathway and had no effect on ACAT1 level. Conclusions: Our study demonstrates, for the first time, that oleacein inhibits foam cell formation in human monocyte-derived macrophages and thus can be a valuable tool in the prevention of early and advanced atherosclerotic lesions.
机译:背景:烯丙是一种塞霉素基团多酚,主要是在L.和L.(oleaceae)中。本研究的目的是探讨荧光素在预防泡沫细胞形成中的潜在作用。材料和方法:从叶子中分离糖。从用粒细胞 - 巨噬细胞刺激因子(GM-CSF)培养的单核细胞获得人单核细胞衍生的巨噬细胞。然后,将细胞与20μM或50μM的烯肽一起温育,并氧化低密度脂蛋白(OXLDL)(50μg/ mL)。使用油红o进行巨噬细胞内脂质沉积的可视化。通过逆转录聚合酶链反应(RT-PCR)和流式细胞术测定CD36,清除剂受体A1(SRE1)和凝集素状的氧化低密度脂蛋白受体1(LOX-1)的表达。通过使用膜蛋白V测定法通过流式细胞仪测定细胞凋亡。 STAT3和酰基辅酶A:通过ELISA测定胆固醇酰基转移酶1(ACAT1)水平。 P-STAT3,P-JAK1,P-JAK2表达式由Western印迹(WB)确定。结果:剂量依赖性方式的糖蛋白酶显着降低巨噬细胞的脂质沉积物以及它们对所选清除剂的表达。与OxLDL和LOX-1受体最低的相比,CD36和SRA1受体的表达最高降低,从高于20%至75%,从约会。 8%到约。 25%与Oxldl刺激的巨噬细胞相比。 Oxldl刺激的巨噬细胞的早期细胞凋亡显着降低(2.5倍)。此外,糖素显着增加了JAK / Stat3途径的蛋白质表达,对ACAT1水平没有影响。结论:我们的研究首次表现出荧光蛋白抑制人单核细胞衍生的巨噬细胞中的泡沫细胞形成,因此可以是预防早期和晚期动脉粥样硬化病变的有价值的工具。

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