Iron and copper promote modification of low density lipoprotein by human arterial smooth muscle cells in culture. (original) (raw)

Find articles by Heinecke, J. in:[JCI](/search/results?q=author.first%5Fname%3A%22J W%22+author.last%5Fname%3A%22Heinecke%22&search%5Ftype=advanced) |PubMed |Google Scholar

Find articles by Rosen, H. in:JCI |PubMed |Google Scholar

Find articles by Chait, A. in:JCI |PubMed |Google Scholar

Published November 1, 1984 -Version history

Abstract

Modification of low density lipoproteins by human arterial smooth muscle cells was characterized by increased electrophoretic mobility and increased content of malondialdehyde-like oxidation products reactive with thiobarbituric acid. Lipoprotein modification was promoted by micromolar concentrations of iron or copper in the culture medium and was metal ion concentration- and time-dependent. The ability of diverse media to promote smooth muscle cell-mediated low density lipoprotein modification correlated with their iron concentration. Therefore, metal ion concentration of culture media contributes substantially to low density lipoprotein modification in vitro. Human monocyte-derived macrophages took up and esterified the cholesterol from modified low density lipoprotein more extensively than from native low density lipoprotein. Metal ion-mediated modification of low density lipoprotein may be a contributing factor to the pathogenesis of arteriosclerosis.

Browse pages

Click on an image below to see the page. View PDF of the complete article