Document Detail


Nonoxidative modifications of lipoproteins in atherogenesis.
MedLine Citation:
PMID:  10448519     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The key initiating event in atherosclerosis is the retention of plasma lipoproteins in the subendothelial matrix. Subsequently, a series of biological responses to this retained material leads to specific molecular and cellular processes that promote lesion formation. There is considerable evidence that many of these biological responses, notably macrophage cholesteryl ester loading (foam cell formation), require subendothelial modification of the retained lipoproteins. Oxidation of lipoproteins is one such modification that likely occurs in vivo and promotes certain atherogenic events, but oxidation cannot explain all aspects of atherogenesis, including certain elements of macrophage foam cell formation. For this reason, there has been renewed interest in other modifications of lipoproteins that may be important in atherogenesis. This review addresses five such lipoprotein modifications, namely aggregation, glycation, immune complex formation, proteoglycan complex formation, and conversion to cholesterol-rich liposomes. The focus is on the evidence that these modifications occur in atherosclerotic lesions and on the potential role of these modified lipoproteins in atherogenesis, with an emphasis on macrophage foam cell formation.
Authors:
I Tabas
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.; Review    
Journal Detail:
Title:  Annual review of nutrition     Volume:  19     ISSN:  0199-9885     ISO Abbreviation:  Annu. Rev. Nutr.     Publication Date:  1999  
Date Detail:
Created Date:  1999-10-04     Completed Date:  1999-10-04     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8209988     Medline TA:  Annu Rev Nutr     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  123-39     Citation Subset:  IM    
Affiliation:
Department of Medicine and Anatomy, Columbia University, New York, New York 10032, USA. iat1@columbia.edu
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MeSH Terms
Descriptor/Qualifier:
Antigen-Antibody Complex
Arteriosclerosis / blood*
Cholesterol / blood
Glycosylation
Humans
Lipoproteins / blood*,  chemistry
Lipoproteins, LDL / blood,  chemistry
Liposomes
Proteoglycans
Grant Support
ID/Acronym/Agency:
HL-56984/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Antigen-Antibody Complex; 0/Lipoproteins; 0/Lipoproteins, LDL; 0/Liposomes; 0/Proteoglycans; 57-88-5/Cholesterol

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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