© 1997 American Heart Association, Inc.
Articles |
Platelet-Activating Factor and Oxidized LDL Induce Immune Activation by a Common Mechanism
From the Department of Medicine, Division of Rheumatology, Karolinska Hospital (J.F., Y.H.H., J.R.), and the Department of Physiological Chemistry, Karolinska Institute (L.S.-E.), Stockholm, Sweden.
Correspondence to Johan Frostegård, Department of Medicine, Division of Rheumatology, Karolinska Hospital, Karolinska Institute, S-17176 Stockholm, Sweden. E-mail johanf{at}rheum.ks.se
Abstract Platelet activating factor (PAF) is a phospholipid with proinflammatory and thrombogenic properties, which has been implicated in inflammatory disorders including vasculitis and asthma. PAF-like compounds are present in oxidized LDL (oxLDL), which has been detected in the atherosclerotic lesion, where it may activate monocytes, macrophages, and T cells. OxLDL may therefore both initiate and perpetuate inflammatory reactions in the artery wall. Herein we demonstrate that PAF has the capacity to induce enhanced interferon gamma (IFN-
) secretion in peripheral blood mononuclear leukocytes (PBMCs), as does oxLDL. Both oxLDL- and PAF-induced IFN- secretions were inhibited by a specific PAF-receptor antagonist, WEB 2170. PAF-like lipids in oxLDL could thus be responsible for oxLDL-induced activation of immune-competent cells. The effects of PAF and oxLDL were inhibited by antibodies to major histocompatibility complex class II and thus depend on accessory cells like monocytes. Both PAF and oxLDL induced tumor necrosis factor-
(TNF-) synthesis in peripheral blood. PAF-mediated TNF- production was inhibited by WEB 2170, whereas oxLDL-induced TNF- was only partially inhibited. These findings indicate that both PAF and oxLDL have the capacity to induce TNF-, which may increase atherogenesis due to its pleiotropic proinflammatory effects. Our findings suggest that the PAF receptor plays an important role in the inflammatory component of atherosclerosis.
Key Words: platelet-activating factor • atherosclerosis • oxidized LDL • tumor necrosis factor • interferon gamma
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