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

Author:

Cimmino Giovanni1,Cirillo Plinio2,Conte Stefano1,Pellegrino Grazia2,Barra Giusi3ORCID,Maresca Lucio4,Morello Andrea2,Calì Gaetano5,Loffredo Francesco16,De Palma Raffaele37,Arena Giulia1,Sawamura Tatsuya8,Ambrosio Giuseppe9,Golino Paolo1ORCID

Affiliation:

1. Department of Translational Medical Sciences, Section of Cardiology, University of Campania “Luigi Vanvitelli”, c/o Monaldi Hospital, Via L. Bianchi, 1, 80131 Naples, Italy

2. Department of Advanced Biomedical Sciences, Section of Cardiology, University of Naples “Federico II”, Naples, Italy

3. Department of Clinical and Experimental Medicine, Section of Clinical Immunology, University of Campania “Luigi Vanvitelli”, Naples, Italy

4. Vascular Surgery Unit, Monaldi Hospital, Naples, Italy

5. Endocrinology and Experimental Oncology Institute, CNR, Naples, Italy

6. Molecular Cardiology, International Centre for Genetic Engineering and Biotechnology, Trieste, Italy

7. Institute of Protein Biochemistry, CNR, Naples, Italy

8. Department of Physiology, Shinshu University School of Medicine, Asahi, Japan

9. Department of Cardiology, University of Perugia, Perugia, Italy

Abstract

Abstract 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.

Funder

Progetti di Ricerca di Interesse Nazionale

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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