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Oxidized LDL-Mediated Monocyte Adhesion to Endothelial Cells Does Not Involve NFκB

Oxidised LDL (oxLDL) is a key pathogenic mediator of atherogenesis, exhibiting many proatherogenic properties. We have examined the effect of oxLDL on monocyte adhesion in the endothelial cell line, EA.hy 926. This has included the role of endothelial cell adhesion molecule expression (ICAM-1 and VC...

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Bibliographic Details
Published in:Biochemical and biophysical research communications 2001-06, Vol.284 (1), p.239-244
Main Authors: Dwivedi, Amrita, Änggård, Erik E., Carrier, Martin J.
Format: Article
Language:English
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Summary:Oxidised LDL (oxLDL) is a key pathogenic mediator of atherogenesis, exhibiting many proatherogenic properties. We have examined the effect of oxLDL on monocyte adhesion in the endothelial cell line, EA.hy 926. This has included the role of endothelial cell adhesion molecule expression (ICAM-1 and VCAM-1), monocyte chemoattractant protein-1 (MCP-1), and the transcription factor NFκB in this interaction. In response to oxLDL (10–100 μg/ml), monocyte adhesion to cells increased dose-dependently. Adhesion of oxLDL at 100 μg/ml was equivalent to that seen with TNFα (10 ng/ml). Unmodified LDL (nLDL, 100 ug/ml) had no effect. Both oxLDL and nLDL increased MCP-1 mRNA levels. Interestingly, oxLDL had no effect on the expression of ICAM-1 and VCAM-1. In addition NFκB was not activated as shown by western blots of IκB-α degradation and electrophoretic mobility shift assay. In summary these data show that increased monocyte adhesion to EA.hy 926 cells occurs independently of ICAM-1, VCAM-1, and NFκB activation and may involve novel adhesive mechanisms.
ISSN:0006-291X
1090-2104
DOI:10.1006/bbrc.2001.4955