Malondialdehyde Conjugated With Albumin Induces Pro-Inflammatory Activation of T Cells Isolated From Human Atherosclerotic Plaques Both Directly and Via Dendritic Cell-Mediated Mechanism

被引:11
|
作者
Rahman, Mizanur [1 ]
Steuer, Johnny [2 ]
Gillgren, Peter [2 ]
Vegvari, Akos [3 ]
Liu, Anquan [1 ]
Frostegard, Johan [1 ]
机构
[1] Karolinska Inst, Inst Environm Med, Stockholm, Sweden
[2] Karolinska Inst, Inst Clin Sci & Educ, Dept Surg, Sect Vasc Surg,Sodersjukhuset, Stockholm, Sweden
[3] Karolinska Inst, Dept Med Biochem & Biophys, Div Chem 1, Biomed, Stockholm, Sweden
来源
JACC-BASIC TO TRANSLATIONAL SCIENCE | 2019年 / 4卷 / 04期
基金
瑞典研究理事会;
关键词
atherosclerosis; dendritic cells; T cells; malondialdehyde; oxidized low-density lipoprotein; LOW-DENSITY-LIPOPROTEIN; SYSTEMIC-LUPUS-ERYTHEMATOSUS; HEAT-SHOCK-PROTEIN; IMMUNE-ACTIVATION; SERUM ANTIBODIES; DEFICIENT MICE; HIGH TITERS; ASSOCIATION; LYMPHOCYTES; INDUCTION;
D O I
10.1016/j.jacbts.2019.03.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Human dendritic cells were differentiated from blood monocytes and treated with malondialdehyde (MDA) conjugated with human serum albumin (HSA). Autologous T cells from human plaques or blood were co-cultured with the pre-treated dendritic cells or treated directly. MDA modifications were studied by mass spectrometry. MDA-HSA induced a pro-inflammatory DC-mediated T-cell activation and also a strong direct effect on T cells, inhibited by an inhibitor of oxidative stress and antibodies against MDA. Atherogenic heat shock protein-60 was strongly induced in T cells activated by MDA-HSA. Two peptide modifications in atherosclerotic patients' HSA were similar to those present in in vitro MDA-modified HSA. (C) 2019 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.
引用
收藏
页码:480 / 494
页数:15
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