Zakiev Emile R, Sobenin Igor A, Sukhorukov Vasily N, Myasoedova Veronika A, Ivanova Ekaterina A, Orekhov Alexander N
Laboratory of Angiopathology, Institute for General Pathology and Pathophysiology.
Laboratory of Angiopathology, Institute for General Pathology and Pathophysiology; Laboratory of Medical Genetics, Russian Cardiology Research and Production Complex, Moscow, Russia.
Vasc Health Risk Manag. 2016 Oct 14;12:379-385. doi: 10.2147/VHRM.S112948. eCollection 2016.
Atherogenic modification of low-density lipoprotein (LDL) plays a crucial role in the pathogenesis of atherosclerosis, as modified LDL, but not native LDL, induces pronounced accumulation of cholesterol and lipids in the arterial wall. It is likely that LDL particles undergo multiple modifications in human plasma: desialylation, changes in size and density, acquisition of negative electric charge, oxidation, and complex formation. In a total LDL preparation isolated from pooled plasma of patients with coronary atherosclerosis and from healthy subjects, two subfractions of LDL could be identified: desialylated LDL bound by a lectin affinity column and normally sialylated (native) LDL that passed through the column. The desialylated LDL subfraction therefore represents circulating modified LDL. In this work, we performed a careful analysis of LDL particles to reveal changes in the composition of glycoconjugates associated with proteins and lipids. Protein fraction of LDL from atherosclerotic patients contained similar amounts of glucosamine, galactose, and mannose, but a 1.6-fold lower level of sialic acid as compared to healthy donors. Lipid-bound glycoconjugates of total LDL from patients with coronary atherosclerosis contained 1.5-2-fold less neutral monosaccharides than total LDL from healthy donors. Patient-derived LDL also contained significantly less sialic acid. Our results demonstrate that carbohydrate composition of LDL from atherosclerotic patients was altered in comparison to healthy controls. In particular, prominent decrease in the sialic acid content was observed. This strengthens the hypothesis of multiple modification of LDL particles in the bloodstream and underscores the clinical importance of desialylated LDL as a possible marker of atherosclerosis progression.
低密度脂蛋白(LDL)的致动脉粥样硬化修饰在动脉粥样硬化的发病机制中起关键作用,因为修饰后的LDL而非天然LDL会促使胆固醇和脂质在动脉壁中显著蓄积。LDL颗粒很可能在人体血浆中经历多种修饰:去唾液酸化、大小和密度改变、获得负电荷、氧化以及形成复合物。在从冠状动脉粥样硬化患者和健康受试者的混合血浆中分离得到的总LDL制剂中,可以鉴定出两种LDL亚组分:通过凝集素亲和柱结合的去唾液酸化LDL以及通过该柱的正常唾液酸化(天然)LDL。因此,去唾液酸化LDL亚组分代表循环中的修饰LDL。在这项研究中,我们对LDL颗粒进行了仔细分析,以揭示与蛋白质和脂质相关的糖缀合物组成的变化。与健康供体相比,动脉粥样硬化患者的LDL蛋白质部分含有相似量的氨基葡萄糖、半乳糖和甘露糖,但唾液酸水平低1.6倍。冠状动脉粥样硬化患者的总LDL的脂质结合糖缀合物中的中性单糖比健康供体的总LDL少1.5至2倍。患者来源的LDL中唾液酸含量也显著更低。我们的结果表明,与健康对照相比,动脉粥样硬化患者的LDL碳水化合物组成发生了改变。特别是,观察到唾液酸含量显著降低。这强化了LDL颗粒在血液中发生多种修饰的假说,并强调了去唾液酸化LDL作为动脉粥样硬化进展可能标志物的临床重要性。