There is growing evidence for the accumulation of phospholipid oxidation pr
oducts (some of which can also be formed enzymatically) in several chronic
disease processes including atherosclerosis. There also is considerable evi
dence that enzymes involved in hydrolysis of these phospholipids (present i
n both lipoproteins and cells) may be important in regulation of atherogene
sis. In vitro studies suggest that these lipids can activate vascular it wa
ll cells to states that contribute to the atherosclerotic process. This rev
iew, focuses on two types of bioactive phospholipids: phosphatidyl cholines
in which the sn-2 fatty acid has been modified by oxidation and lysophosph
atidic acid in it which both the sn-2 and sn-3 positions have been modified
. The mechanism by which these phospholipid oxidation products activate cel
ls has revealed the presence of several different receptors and signal tran
sduction pathways. (C) 2001, Elsevier Science Inc.