Evidence for a dominant role of lipoxygenase(s) in the oxidation of LDL by mouse peritoneal macrophages

It has been suggested that the oxidative modification of low density lipoprotein (LDL) is a key event in atherogenesis. Several mechanisms have been proposed to explain how different types of cells modify LDL. In this study we examine the relative contributions of superoxide anions and cellular lipo...

Full description

Bibliographic Details
Main Authors: SM Rankin, S Parthasarathy, D Steinberg
Format: Article
Language:English
Published: Elsevier 1991-03-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520420681
id doaj-e121db3d30d340b6a90c49e12047f813
record_format Article
spelling doaj-e121db3d30d340b6a90c49e12047f8132021-04-25T04:21:38ZengElsevierJournal of Lipid Research0022-22751991-03-01323449456Evidence for a dominant role of lipoxygenase(s) in the oxidation of LDL by mouse peritoneal macrophagesSM Rankin0S Parthasarathy1D Steinberg2Department of Medicine, University of California, San Diego, La Jolla 92093.Department of Medicine, University of California, San Diego, La Jolla 92093.Department of Medicine, University of California, San Diego, La Jolla 92093.It has been suggested that the oxidative modification of low density lipoprotein (LDL) is a key event in atherogenesis. Several mechanisms have been proposed to explain how different types of cells modify LDL. In this study we examine the relative contributions of superoxide anions and cellular lipoxygenase (LO) in the modification of LDL by macrophages. Superoxide dismutase (SOD) inhibited LDL oxidation by macrophages but only by 25%. Under the same conditions, several LO inhibitors (eicosatetraynoic acid (ETYA), piriprost, and A-64077) almost completely inhibited the modification of LDL by macrophages. SOD had a greater inhibitory effect on the modification of LDL by U937 cells and fibroblasts (32% and 64%, respectively) but again LO inhibitors had a much greater effect (79 to 100% inhibition). Incubation of [1-14C]linoleic acid with mouse peritoneal macrophages resulted in its conversion to a single more polar product coeluting with 13- and 9-HODE by reverse phase HPLC. When the cells were preincubated with LO inhibitors, formation of this product was significantly inhibited. It is concluded that the modification of LDL by macrophages is mediated in large part by lipoxygenase-type activity.http://www.sciencedirect.com/science/article/pii/S0022227520420681
collection DOAJ
language English
format Article
sources DOAJ
author SM Rankin
S Parthasarathy
D Steinberg
spellingShingle SM Rankin
S Parthasarathy
D Steinberg
Evidence for a dominant role of lipoxygenase(s) in the oxidation of LDL by mouse peritoneal macrophages
Journal of Lipid Research
author_facet SM Rankin
S Parthasarathy
D Steinberg
author_sort SM Rankin
title Evidence for a dominant role of lipoxygenase(s) in the oxidation of LDL by mouse peritoneal macrophages
title_short Evidence for a dominant role of lipoxygenase(s) in the oxidation of LDL by mouse peritoneal macrophages
title_full Evidence for a dominant role of lipoxygenase(s) in the oxidation of LDL by mouse peritoneal macrophages
title_fullStr Evidence for a dominant role of lipoxygenase(s) in the oxidation of LDL by mouse peritoneal macrophages
title_full_unstemmed Evidence for a dominant role of lipoxygenase(s) in the oxidation of LDL by mouse peritoneal macrophages
title_sort evidence for a dominant role of lipoxygenase(s) in the oxidation of ldl by mouse peritoneal macrophages
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1991-03-01
description It has been suggested that the oxidative modification of low density lipoprotein (LDL) is a key event in atherogenesis. Several mechanisms have been proposed to explain how different types of cells modify LDL. In this study we examine the relative contributions of superoxide anions and cellular lipoxygenase (LO) in the modification of LDL by macrophages. Superoxide dismutase (SOD) inhibited LDL oxidation by macrophages but only by 25%. Under the same conditions, several LO inhibitors (eicosatetraynoic acid (ETYA), piriprost, and A-64077) almost completely inhibited the modification of LDL by macrophages. SOD had a greater inhibitory effect on the modification of LDL by U937 cells and fibroblasts (32% and 64%, respectively) but again LO inhibitors had a much greater effect (79 to 100% inhibition). Incubation of [1-14C]linoleic acid with mouse peritoneal macrophages resulted in its conversion to a single more polar product coeluting with 13- and 9-HODE by reverse phase HPLC. When the cells were preincubated with LO inhibitors, formation of this product was significantly inhibited. It is concluded that the modification of LDL by macrophages is mediated in large part by lipoxygenase-type activity.
url http://www.sciencedirect.com/science/article/pii/S0022227520420681
work_keys_str_mv AT smrankin evidenceforadominantroleoflipoxygenasesintheoxidationofldlbymouseperitonealmacrophages
AT sparthasarathy evidenceforadominantroleoflipoxygenasesintheoxidationofldlbymouseperitonealmacrophages
AT dsteinberg evidenceforadominantroleoflipoxygenasesintheoxidationofldlbymouseperitonealmacrophages
_version_ 1721510381907607552