Oxidized low-density lipoproteins induce tissue factor expression in T-lymphocytes via activation of lectin-like oxidized low-density lipoprotein receptor-1

被引:18
|
作者
Cimmino, Giovanni [1 ]
Cirillo, Plinio [2 ]
Conte, Stefano [1 ]
Pellegrino, Grazia [2 ]
Barra, Giusi [3 ]
Maresca, Lucio [4 ]
Morello, Andrea [2 ]
Cali, Gaetano [5 ]
Loffredo, Francesco [1 ,6 ]
De Palma, Raffaele [3 ,7 ]
Arena, Giulia [1 ]
Sawamura, Tatsuya [8 ]
Ambrosio, Giuseppe [9 ]
Golino, Paolo [1 ]
机构
[1] Univ Campania Luigi Vanvitelli, Sect Cardiol, Dept Translat Med Sci, Monaldi Hosp, Via L Bianchi 1, I-80131 Naples, Italy
[2] Univ Naples Federico II, Sect Cardiol, Dept Adv Biomed Sci, Naples, Italy
[3] Univ Campania Luigi Vanvitelli, Sect Clin Immunol, Dept Clin & Expt Med, Naples, Italy
[4] Monaldi Hosp, Vasc Surg Unit, Naples, Italy
[5] CNR, Endocrinol & Expt Oncol Inst, Naples, Italy
[6] Int Ctr Genet Engn & Biotechnol, Mol Cardiol, Trieste, Italy
[7] CNR, Inst Prot Biochem, Naples, Italy
[8] Shinshu Univ, Sch Med, Dept Physiol, Asahi, Japan
[9] Univ Perugia, Dept Cardiol, Perugia, Italy
关键词
Lipoproteins; Atherosclerosis; Inflammation; T-lymphocyte; Tissue factor; HUMAN ATHEROSCLEROTIC PLAQUES; ACUTE CORONARY SYNDROMES; OXIDATIVE STRESS; CELL-ACTIVATION; LOX-1; INHIBITION; IMMUNITY; INFLAMMATION; BIOLOGY; PLAYERS;
D O I
10.1093/cvr/cvz230
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims T-lymphocytes plays an important role in the pathophysiology of acute coronary syndromes. T-cell activation in vitro by pro-inflammatory cytokines may lead to functional tissue factor (TF) expression, indicating a possible contribution of immunity to thrombosis. Oxidized low-density lipoproteins (oxLDLs) are found abundantly in atherosclerotic plaques. We aimed at evaluating the effects of oxLDLs on TF expression in T cells and the role of the lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1). Methods and results CD3(+) cells were isolated from healthy volunteers. Gene, protein, and surface expression of TF, as well as of LOX-1, were assessed at different time-points after oxLDL stimulation. To determine whether oxLDL-induced TF was LOX-1 dependent, T cells were pre-incubated with an LOX-1 inhibiting peptide (L-RBP) or with an anti-LOX-1 blocking antibody. To exclude that TF expression was mediated by reactive oxygen species (ROS) generation, oxLDL-stimulated T cells were pre-incubated with superoxide dismutase + catalase or with 4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (Tempol), an intracellular free radical scavenger. Finally, to determine if the observed findings in vitro may have a biological relevance, the presence of CD3(+)/TF+/LOX-1(+) cells was evaluated by immunofluorescence in human carotid atherosclerotic lesions. oxLDLs induced functionally active TF expression in T cells in a dose- and time-dependent manner, independently on ROS generation. No effect was observed in native LDL-treated T cells. LOX-1 expression was also induced by oxLDLs in a time- and dose-dependent manner. Pre-incubation with L-RBP or anti-LOX-1 antibody almost completely inhibited oxLDL-mediated TF expression. Interestingly, human carotid plaques showed significant infiltration of CD3(+) cells (mainly CD8(+) cells), some of which were positive for both TF and LOX-1. Conclusion oxLDLs induce functional TF expression in T-lymphocytes in vitro via interaction of oxLDLs with LOX-1. Human carotid atherosclerotic plaques contain CD3(+)/CD8(+)cells that express both TF and LOX-1, indicating that also in patients these mechanisms may play an important role.
引用
收藏
页码:1125 / 1135
页数:11
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