LDL oxidation by activated monocytes: characterization of the oxidized LDL and requirement for transition metal ions
Monocytes can be activated by incubation with opsonized zymosan (Zop), and under these conditions can oxidize low density lipoprotein (LDL). We have characterized the biochemical changes in the lipoprotein after this oxidation. We found that monocyte-oxidized LDL has increased mobility on agarose ge...
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1998-11-01
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doaj-f4c0b350422e47f0a8438840d1172ec42021-04-26T05:45:57ZengElsevierJournal of Lipid Research0022-22751998-11-01391122012208LDL oxidation by activated monocytes: characterization of the oxidized LDL and requirement for transition metal ionsXiaoyan Xing0Joanne Baffic1Carl P. Sparrow2Department of Lipid Biochemistry, Merck Research Laboratories, 126 E. Lincoln Avenue, Rahway, NJ 07065Department of Lipid Biochemistry, Merck Research Laboratories, 126 E. Lincoln Avenue, Rahway, NJ 07065To whom correspondence should be addressed.; Department of Lipid Biochemistry, Merck Research Laboratories, 126 E. Lincoln Avenue, Rahway, NJ 07065Monocytes can be activated by incubation with opsonized zymosan (Zop), and under these conditions can oxidize low density lipoprotein (LDL). We have characterized the biochemical changes in the lipoprotein after this oxidation. We found that monocyte-oxidized LDL has increased mobility on agarose gels, increased absorbance at 234 nm, increased content of lysophosphatidylcholine, and fluorescence at 430 nm when excited at 350 nm. All these features were somewhat less pronounced in monocyte-oxidized LDL than in LDL oxidized by 5 μm CuSO4. Under appropriate conditions, Zop-stimulated monocytes oxidized LDL to a form recognized by macrophage scavenger receptors. Monocytes stimulated by Zop produced superoxide and also oxidized LDL, whereas monocytes stimulated by phorbol ester produced slightly more superoxide but did not oxidize LDL. We found that the chelators EDTA and diethylenetriaminepentaacetic acid inhibited LDL oxidation by Zop-stimulated monocytes, implying a requirement for transition metal ions. We found that Zop contained approximately 5 nmol iron per mg, probably as Fe3+. Zop stripped of its iron supported superoxide production by monocytes, but did not support LDL oxidation. Furthermore, Fe2+ appeared in the medium when monocytes were incubated with Zop, but not with iron-stripped Zop. Taken together, these results imply that monocytes stimulated by Zop are able to oxidize LDL only because of contaminating iron in the commercial zymosan preparations. —Xing, X., J. Baffic, and C. P. Sparrow. LDL oxidation by activated monocytes: characterization of the oxidized LDL and requirement for transition metal ions. J. Lipid. Res. 1998. 39: 2201–2208.http://www.sciencedirect.com/science/article/pii/S0022227520324755scavenger receptoratherosclerosisironcholesterolzymosansuperoxide |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xiaoyan Xing Joanne Baffic Carl P. Sparrow |
spellingShingle |
Xiaoyan Xing Joanne Baffic Carl P. Sparrow LDL oxidation by activated monocytes: characterization of the oxidized LDL and requirement for transition metal ions Journal of Lipid Research scavenger receptor atherosclerosis iron cholesterol zymosan superoxide |
author_facet |
Xiaoyan Xing Joanne Baffic Carl P. Sparrow |
author_sort |
Xiaoyan Xing |
title |
LDL oxidation by activated monocytes: characterization of the oxidized LDL and requirement for transition metal ions |
title_short |
LDL oxidation by activated monocytes: characterization of the oxidized LDL and requirement for transition metal ions |
title_full |
LDL oxidation by activated monocytes: characterization of the oxidized LDL and requirement for transition metal ions |
title_fullStr |
LDL oxidation by activated monocytes: characterization of the oxidized LDL and requirement for transition metal ions |
title_full_unstemmed |
LDL oxidation by activated monocytes: characterization of the oxidized LDL and requirement for transition metal ions |
title_sort |
ldl oxidation by activated monocytes: characterization of the oxidized ldl and requirement for transition metal ions |
publisher |
Elsevier |
series |
Journal of Lipid Research |
issn |
0022-2275 |
publishDate |
1998-11-01 |
description |
Monocytes can be activated by incubation with opsonized zymosan (Zop), and under these conditions can oxidize low density lipoprotein (LDL). We have characterized the biochemical changes in the lipoprotein after this oxidation. We found that monocyte-oxidized LDL has increased mobility on agarose gels, increased absorbance at 234 nm, increased content of lysophosphatidylcholine, and fluorescence at 430 nm when excited at 350 nm. All these features were somewhat less pronounced in monocyte-oxidized LDL than in LDL oxidized by 5 μm CuSO4. Under appropriate conditions, Zop-stimulated monocytes oxidized LDL to a form recognized by macrophage scavenger receptors. Monocytes stimulated by Zop produced superoxide and also oxidized LDL, whereas monocytes stimulated by phorbol ester produced slightly more superoxide but did not oxidize LDL. We found that the chelators EDTA and diethylenetriaminepentaacetic acid inhibited LDL oxidation by Zop-stimulated monocytes, implying a requirement for transition metal ions. We found that Zop contained approximately 5 nmol iron per mg, probably as Fe3+. Zop stripped of its iron supported superoxide production by monocytes, but did not support LDL oxidation. Furthermore, Fe2+ appeared in the medium when monocytes were incubated with Zop, but not with iron-stripped Zop. Taken together, these results imply that monocytes stimulated by Zop are able to oxidize LDL only because of contaminating iron in the commercial zymosan preparations. —Xing, X., J. Baffic, and C. P. Sparrow. LDL oxidation by activated monocytes: characterization of the oxidized LDL and requirement for transition metal ions. J. Lipid. Res. 1998. 39: 2201–2208. |
topic |
scavenger receptor atherosclerosis iron cholesterol zymosan superoxide |
url |
http://www.sciencedirect.com/science/article/pii/S0022227520324755 |
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