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EXTENSIVE NITRATION OF PROTEIN TYROSINES IN HUMAN ATHEROSCLEROSIS DETECTED BY IMMUNOHISTOCHEMISTRY
Author(s): BECKMANN JS, YE YZ, ANDERSON PG, CHEN J, ACCAVITTI MA, TARPEY MM, WHITE CR, BECKMAN JS
Source: BIOLOGICAL CHEMISTRY HOPPE-SEYLER    Volume: 375    Issue: 2    Pages: 81-88    Published: FEB 1994  
Times Cited: 895     References: 20     
Abstract: Oxidation of lipoproteins is important for the initiation and propagation of the atherosclerotic lesion and may involve secondary oxidants derived from nitric oxide. Nitric oxide (NO) reacts at near diffusion limited rates with superoxide (O-2.(-)) to form the strong oxidant, peroxynitrite (ONOO-). Nitration on the ortho position of tyrosine is a major product of peroxynitrite attack on proteins. Nitrotyrosine was detected in atherosclerotic lesions of formalin-fixed human coronary arteries with polyclonal and monoclonal antibodies. Binding was pronounced in and around foamy macrophages within the atheroma deposits. Nitration was also observed in early subintimal fatty streaks. Antibody binding was completely blocked by co-incubation with 10mM nitrotyrosine, but not by equivalent concentrations of aminotyrosine or phosphotyrosine. The presence of nitrotyrosine indicates that oxidants derived from nitric oxide such as peroxynitrite are generated in human atherosclerosis and may be involved in its pathogenesis.
Document Type: Article
Language: English
Reprint Address: BECKMAN, JS (reprint author), UNIV ALABAMA, DEPT ANESTHESIOL, BIRMINGHAM, AL 35233 USA
Addresses:
1. UNIV ALABAMA, DEPT PEDIAT, BIRMINGHAM, AL 35233 USA
2. UNIV ALABAMA, DEPT MED, BIRMINGHAM, AL 35233 USA
Publisher: WALTER DE GRUYTER & CO, GENTHINER STRASSE 13, D-10785 BERLIN, GERMANY
Subject Category: Biochemistry & Molecular Biology
IDS Number: MZ178
ISSN: 0177-3593
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