Author/Authors :
Mahmoudi, Mohammad Jafar Division of Cardiology - Department of Internal Medicine - School of Medicine , Mahmoudi, Maryam Department of Nutrition and Biochemistry , Siassi, Fereydoon Department of Nutrition and Biochemistry , Chahardoli, Reza Department of Nutrition and Biochemistry , Saboor-Yaraghi, Ali-Akbar Department of Nutrition and Biochemistry , Shokri, Fazel Department of Immunology , Khoshnoodi, Jalal Department of Immunology , Eshraghian, Mohammad Reza Department of Epidemiology and Biostatistics - School of Public Health - Tehran University of Medical Sciences , Zarnani, Amir Hassan Nanobiotechnology Research Center - Avicenna Research Institute - ACECR , Hedayat, Mona Molecular Immunology Research Center - School of Medicine - Tehran University of Medical Sciences , Rezaei, Nima Molecular Immunology Research Center - School of Medicine - Tehran University of Medical Sciences , Nayeri, Hashem Falavarjan Islamic Azad University - Falavarjan - Isfahan
Abstract :
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 (p<0.001) 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.
Keywords :
Peripheral Blood Mononuclear Cells , oxLDL , Cytotoxicity , Atherosclerosis