Literature DB >> 17065664

High density lipoprotein subfractions: isolation, composition, and their duplicitous role in oxidation.

Peter A C McPherson1, Ian S Young, Bronac McKibben, Jane McEneny.   

Abstract

The plasma HDLs represent a major class of cholesterol-transporting lipoprotein that can be divided into two distinct subfractions, HDL(2) and HDL(3), by ultracentrifugation. Existing methods for the subfractionation of HDL requires lengthy ultracentrifugations, making them unappealing for large-scale studies. We describe a method that subfractionates HDL from plasma in only 6 h, representing a substantial decrease in total isolation time. The subfractions so isolated were assessed for a variety of lipid and protein components, in addition to their susceptibility to oxidation, both alone and in combination with VLDL and LDL. We report for the first time a prooxidant role for HDL during VLDL oxidation, in which HDL donates preformed hydroperoxides to VLDL in a cholesteryl ester transfer protein (CETP)-dependent process. Examination of the participation of HDL in LDL oxidation has reinforced its classic role as a potent antioxidant. Furthermore, we have also implicated the second major HDL-associated enzyme, LCAT, in these processes, whereby it acts as a potent prooxidant during VLDL oxidation but as an antioxidant during LDL oxidation. Thus, we have identified a potentially duplicitous role for HDL in the pathogenesis of atherosclerosis, attributable to both CETP and LCAT.

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Year:  2006        PMID: 17065664     DOI: 10.1194/jlr.M600094-JLR200

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  30 in total

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3.  Serum amyloid A levels are associated with polymorphic variants in the serum amyloid A 1 and 2 genes.

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Review 4.  Regulation of ABCA1 functions by signaling pathways.

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5.  Associations between follicular fluid high density lipoprotein particle components and embryo quality among in vitro fertilization patients.

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8.  High-density lipoprotein inhibits human M1 macrophage polarization through redistribution of caveolin-1.

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Journal:  Bioinformatics       Date:  2009-04-05       Impact factor: 6.937

Review 10.  Dysfunctional HDL as a diagnostic and therapeutic target.

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