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Lymphocyte Cytotoxicity of oxLDL in Patients with Atherosclerosis

机译:oxLDL对动脉粥样硬化患者的淋巴细胞毒性

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Background: Atherosclerosis, a chronic inflammatory disease of the vessel wall is characterized by local and systemic immune responses to a variety of antigens. Oxidized low-density lipoprotein (oxLDL) is considered as an important determining factor in the pathogenesis of atherosclerosis. Objective: The purpose of this study was to investigate the degree of peripheral blood mononuclear cells (PBMC) vulnerability to in vitro oxLDL-induced cytotoxicity from atherosclerotic patients in comparison to healthy individuals. Methods: Thirty patients with atherosclerotic lesions, confirmed by angiography, and 30 matched healthy individuals were investigated. PBMC was prepared from individuals' blood samples which were further stimulated with low dose (1 μg/mL) and high dose (50 μg/mL) of extensively oxidized LDL. MTT assay was utilized to measure cell viability and proliferation. Stimulation index (SI) was calculated as mean ratio of optical density (OD) of the stimulated cells divided by OD of untreated cells. Results: Low dose oxLDL treatment caused no significant proliferative or cytotoxic effect in the control group; however, similar treatment caused significant cytotoxic effect in the patient group compared to the controls (p=0.026). High dose oxLDL treatment induced more significant cytotoxicity in the patient compared to the control group (p=0.006). Comparison of the SI between the two groups of patients and controls showed significantly lower index by either the low (p=0.03) or the high dose (p0.001) oxLDL in the patients compared to the controls. Conclusions: PBMC from patients with atherosclerosis showed increased susceptibility to oxLDL-induced cytotoxicity. Our results imply that prolonged exposure to elevated levels of circulating oxLDL could weaken the cellular defense mechanisms by progressive depletion of the pool of antiapoptotic proteins, rendering the cells more vulnerable to oxLDL-induced cell death.
机译:背景:动脉粥样硬化是一种血管壁的慢性炎性疾病,其特征在于对多种抗原的局部和全身免疫反应。氧化的低密度脂蛋白(oxLDL)被认为是动脉粥样硬化发病机理的重要决定因素。目的:本研究的目的是与健康个体相比,研究动脉粥样硬化患者外周血单核细胞(PBMC)对体外oxLDL诱导的细胞毒性的易感性程度。方法:30例经血管造影证实的动脉粥样硬化病变患者和30例健康人进行了调查。 PBMC是从个人的血液样本中制备的,然后分别用低剂量(1μg/ mL)和高剂量(50μg/ mL)的广泛氧化LDL刺激。使用MTT测定法测量细胞活力和增殖。刺激指数(SI)计算为刺激细胞的光密度(OD)的平均比除以未处理细胞的OD。结果:低剂量的oxLDL治疗在对照组中没有引起明显的增殖或细胞毒性作用。然而,与对照组相比,类似的治疗在患者组中引起了明显的细胞毒性作用(p = 0.026)。与对照组相比,高剂量oxLDL治疗在患者中诱导出更显着的细胞毒性(p = 0.006)。两组患者和对照组之间的SI比较显示,与对照组相比,患者的低(p = 0.03)或高剂量(p <0.001)oxLDL指数显着降低。结论:动脉粥样硬化患者的PBMC对oxLDL诱导的细胞毒性的敏感性增加。我们的结果表明,长时间暴露于升高水平的循环oxLDL可能会通过逐渐耗尽抗凋亡蛋白池而削弱细胞防御机制,从而使细胞更容易受到oxLDL诱导的细胞死亡的影响。

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