OXIDATION OF CHOLESTEROL MOIETY OF LOW-DENSITY-LIPOPROTEIN IN THE PRESENCE OF HUMAN ENDOTHELIAL-CELLS OR CU+2 IONS - IDENTIFICATION OF MAJOR PRODUCTS AND THEIR EFFECTS

Oxidation of lipoproteins is believed to play a key role in atherogenesis. In this study, low density lipoproteins (LDL) was subjected to oxidation in the presence of either human umbilical vein endothelial cells or with Cu+2 ions and the major oxides formed were identified. While cholesterol-α-epoxide (C-αEP) was the major product of cholesterol peroxidation in the presence of endothelial cells, cholest-3,5-dien-7-one (CD) predominated in the presence of Cu+2 ion. Both steroids were identified by gas chromatography/mass spectrometry. HDL cholesterol was resistant to oxidation. When tested on human skin fibroblasts in culture C-αEP (10 μg/ml) caused marked stimulation of 14C-oleate incorporation into cholesterol esters, while CD stimulated cholesterol esterification only mildly. These studies show that a) C-αEP is the major peroxidation product of LDL cholesterol moiety in the presence of endothelial cells and b) it causes marked stimulation of cholesterol esterification in cells. C-αEP may play a key role in increasing cholesterol esterification noted in atherogenesis. © 1991.