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首页> 外文期刊>Journal of Biomechanics >Oxidized low-density lipoprotein (Ox-LDL) impacts on erythrocyte viscoelasticity and its molecular mechanism.
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Oxidized low-density lipoprotein (Ox-LDL) impacts on erythrocyte viscoelasticity and its molecular mechanism.

机译:氧化的低密度脂蛋白(Ox-LDL)对红细胞粘弹性及其分子机制的影响。

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摘要

The oxidized low-density lipoprotein (Ox-LDL) plays an important role in atherosclerosis, yet it remains unclear if it damages circulating erythrocytes. In this study, erythrocyte deformability and its membrane proteins after Ox-LDL incubations are investigated by micropipette aspiration, thiol radical measurement, and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE). Results show that Ox-LDL incubation reduces the erythrocyte deformability, decreases free thiol radical contents in erythrocytes, and induces the cross-linking among membrane proteins. SDS-PAGE analysis reveals a high molecular weight (HMW) complex as well as new bands between spectrins and band 3 and reduced ratios between band 3 and other major membrane skeletal proteins. Analyses indicate that Ox-LDL makes erythrocytes harder to deform through a molecular mechanism by which the oxidation of free thiol radicals forms disulfide bonds among membrane skeletal proteins.
机译:氧化的低密度脂蛋白(Ox-LDL)在动脉粥样硬化中起着重要作用,但尚不清楚它是否损害循环中的红细胞。在这项研究中,通过微量移液器抽吸,硫醇自由基测量和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)研究了Ox-LDL孵育后的红细胞变形能力及其膜蛋白。结果表明,Ox-LDL孵育降低了红细胞的可变形性,降低了红细胞中的游离巯基含量,并诱导了膜蛋白之间的交联。 SDS-PAGE分析揭示了高分子量(HMW)复合物,以及在光谱与条带3之间的新条带以及在条带3与其他主要膜骨骼蛋白之间的比率降低。分析表明,Ox-LDL通过分子机制使红细胞更难变形,通过这种分子机制,游离硫醇基的氧化在膜骨架蛋白之间形成了二硫键。

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