Journal
ATHEROSCLEROSIS
Volume 160, Issue 2, Pages 281-288Publisher
ELSEVIER SCI IRELAND LTD
DOI: 10.1016/S0021-9150(01)00582-2
Keywords
monocytes; cell-to-cell interaction; inflammation; adhesion molecules; lipid mediators
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Inflammatory and immune responses are highly relevant processes in the pathogenesis of atherosclerosis. as illustrated by the central event of monocyte accumulation in atherosclerotic plaques. Integrin LFA-1-mediated adhesion of circulating monocytes to the endothelium is a prerequisite for recruitment of monocytes to these areas. Integrin-mediated adhesion is tightly regulated and integrins are only Functional in response to particular monocyte activation stimuli. We investigated the role of oxidized low-density lipoprotein (LDL) in adhesion of resting monocytes prepared by elutriation front endothelium. Our results showed that: (1) oxidized LDL (and MCP-1) induced both LFA-1-mediated adhesion of monocytes to endothelial cells and transendothelial migration of monocytes; (2) oxidized LDL functionally transformed monocyte LFA-1 to an activated form: (3) oxidized LDL induced F-actin polymerization and cytoskeletal rearrangement within seconds; and (4) the LDL-associated antioxidant. chi-toeopherol, but not beta-tocopherol, inhibited both F-actin polymerization and LFA-1-mediated adhesion of monocytes, which paralleled the effect of protein kinase C (PKC) inhibitors. Our results indicate that oxidized LDL plays a pivotal role in triggering LFA-1 activation and LFA-1-mediated adhesion rind transmigration of monocytes to sites of atherosclerotic plaques. via the PKC pathway. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
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