Abstract
It has been proposed that low density lipoprotein (LDL) must undergo oxidative modification before it can give rise to foam cells, the key component of the fatty streak lesion of atherosclerosis. Oxidation of LDL probably generates a broad spectrum of conjugates between fragments of oxidized fatty acids and apolipoprotein B. We now present three mutually supportive lines of evidence for oxidation of LDL in vivo: (i) Antibodies against oxidized LDL, malondialdehyde-lysine, or 4-hydroxynonenal-lysine recognize materials in the atherosclerotic lesions of LDL receptor-deficient rabbits; (ii) LDL gently extracted from lesions of these rabbits is recognized by an antiserum against malondialdehyde-conjugated LDL; (iii) autoantibodies against malondialdehyde-LDL (titers from 512 to greater than 4096) can be demonstrated in rabbit and human sera.
MeSH Terms
Alkaline Phosphatase/metabolism
Animals
Antibodies
Antigen-Antibody Complex/analysis
Aorta, Thoracic/metabolism,pathology
Arteriosclerosis/metabolism,pathology
Autoantibodies/immunology
Epitopes/analysis
Guinea Pigs
Humans
Hyperlipidemias/metabolism
Immunoenzyme Techniques
Lipoproteins, LDL/blood,immunology,metabolism
Male
Malonates/analysis
Malondialdehyde/analysis,immunology
Mice
Oxidation-Reduction
Rabbits
Radioimmunoassay
Reference Values
Chemicals
Antibodies
Antigen-Antibody Complex
Autoantibodies
Epitopes
Lipoproteins, LDL
Malonates
Malondialdehyde
Alkaline Phosphatase
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Palinski W
Department of Medicine, University of California, San Diego, La Jolla 92093.
Rosenfeld M E
Ylä-Herttuala S
Gurtner G C
Socher S S
Butler S W
Parthasarathy S
Carew T E
Steinberg D
Witztum J L
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