Department of Vascular Surgery, The Third Bethune Hospital of Jilin University, Changchun, China.
Department of Endocrinology, Sanmenxia Central Hospital, Sanmenxia, China.
Minerva Med. 2019 Apr;110(2):107-114. doi: 10.23736/S0026-4806.18.05711-7. Epub 2018 Oct 29.
Foam cells are characteristic pathologic cells of atherosclerosis (AS), they are lipid-loaded macrophages present on atherosclerotic lesions. A large number of studies has shown that the pathogenesis of AS is the result of interactions between the lipid metabolism disorders and chronic inflammatory responses in the body. Albiflorin can inhibit the inflammatory response and it has shown a therapeutic effect on certain inflammatory diseases.
In this study, a human acute monocytic leukemia cell line (THP-1)-derived foam cell model was established via oxidized low-density lipoprotein (ox-LDL) to observe the effects of albiflorin on the AS-characteristic foam cells.
Our results showed that, after the treatment with ox-LDL, macrophages induced by propylene glycol methyl ether acetate (PMA), presented large amounts of lipid deposition in their cytoplasm, indicating that the THP-1-derived foam cell model was successfully established. On the other hand, the same cells pretreated with albiflorin presented significantly reduced amounts of lipid deposition, and their contents of total cholesterol and triglyceride were also clearly lower. Besides, the expression levels of low-density lipoprotein receptor-1 (LOX-1) and nuclear factor-κB (NF-κB) were significantly decreased, and the expression levels of downstream factors interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) were also obviously decreased in the cells treated with albiflorin but not in the negative control cells. Moreover, after treatment of macrophages with different concentrations of ox-LDL, the expression levels of LOX-1 and NF-κB were up-regulated in an ox-LDL concentration-dependent manner, and so were the expression levels of IL-6 and TNF-α. And, it was found after treatment with LOX-1 neutralizing antibody or NF-κB inhibitor (during the foam cell formation induction via ox-LDL) that the lipid deposition in the cytoplasm of the cells was reduced, as in the cells treated with albiflorin.
Taken together, our findings suggest that albiflorin decreases lipid deposition in the cytoplasm and blocks the foaming process by regulating the LOX-1/NF-κB signaling pathway.
泡沫细胞是动脉粥样硬化(AS)的特征性病理细胞,是存在于动脉粥样硬化病变中的富含脂质的巨噬细胞。大量研究表明,AS 的发病机制是机体脂质代谢紊乱和慢性炎症反应相互作用的结果。梓醇可以抑制炎症反应,对某些炎症性疾病具有治疗作用。
本研究通过氧化型低密度脂蛋白(ox-LDL)建立人急性单核细胞白血病细胞系(THP-1)衍生的泡沫细胞模型,观察梓醇对 AS 特征性泡沫细胞的作用。
结果显示,经丙二醇甲醚乙酸酯(PMA)诱导的巨噬细胞用 ox-LDL 处理后,细胞浆内出现大量脂质沉积,表明 THP-1 衍生的泡沫细胞模型成功建立。另一方面,用梓醇预处理的相同细胞,其脂质沉积量明显减少,总胆固醇和甘油三酯含量也明显降低。此外,用梓醇处理的细胞中,低密度脂蛋白受体-1(LOX-1)和核因子-κB(NF-κB)的表达水平明显降低,下游因子白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的表达水平也明显降低,但阴性对照组细胞则无此现象。此外,用不同浓度 ox-LDL 处理巨噬细胞后,LOX-1 和 NF-κB 的表达水平呈 ox-LDL 浓度依赖性上调,IL-6 和 TNF-α的表达水平也随之上调。用 LOX-1 中和抗体或 NF-κB 抑制剂(在 ox-LDL 诱导泡沫细胞形成过程中)处理后发现,细胞浆内的脂质沉积减少,与梓醇处理的细胞相似。
综上所述,本研究结果表明,梓醇通过调节 LOX-1/NF-κB 信号通路减少细胞浆内脂质沉积,阻断泡沫化过程。