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Role of oxidatively modified LDL in atherosclerosis

  • Urs P. Steinbrecher(corresponding author)
    ,
  • Hanfang Zhang
    ,
  • Marilee Lougheed
*Corresponding author for this work
  • University of British Columbia
Scholary Output:
Contribution to journal
Article
Research
Peer-review

Abstract

Oxidative modification of LDL is accompanied by a number of compositional and structural changes, including increased electrophoretic mobility, increased density, fragmentation of apolipoprotein B, hydrolysis of phosphatidylcholine, derivatization of lysine amino groups, and generation of lfuorescent adducts due to covalent binding of lipid oxidation products to apo B. In addition, oxidation of LDL has been shown to result in numerous changes in its biologic properties that could have pathogenetic imortance, including accelerated uptake in macrophages, cytotoxicity, and chemotactic activity for monocytes. The present article summarrizes very recent developments related to the mechanism of oxidation of LDL by cells, receptor-mediated uptake of oxidized LDL in macrophages, the mechanism of phosphatidylcholine hydrolysis during LDL oxidation, and other biologic actions of oxidized LDL including cytotoxicity, altered eicosanoid metabolism, and effects on the secretion of growth factors and chemotactic factors. In addition, this review will exzmine the evidence for the presence of oxidized LDL in vivo and the evidence that oxidized LDL plays a pathogenetic role in atherosclerosis.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Research
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 155-168 (14 pages)

Journal (Volume, Issue Number)

Free Radical Biology and Medicine (Volume 9, Issue 2)

Publication milestones

  • Published - 1990

Publication status

Published - 1990

ISSN

0891-5849

Publication IDs

  • Scopus: 0024992023
  • PubMed: 2227530

Publication metrics

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Scopus
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1
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0.33
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2
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0.67
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1
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1

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Funding Details

Acknowledgements--The authors are Indebted to many colleagues and collaborators for stimulating discussions and advice, but wish to express particular appreciation to Drs Joseph L Witztum, Alan Chalt, Guy Chlsolm, Alan Attle, Sampath Parthasarathy. Michael Rosenfeld, Margaret Haberland, and Daniel Steinberg Studies from our laboratory were supported by grants from the Medical Research Council of Canada, the B C Y Heart Foundation, and the B C Health Care Research Foundation
FundersFunding numbers
B C Health Care Research Foundation
-
B C Y Heart Foundation
-
MRC
-