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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.
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页码:1125 / 1135
页数:11
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