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

被引:64
作者
McPherson, Peter A. C. [1 ]
Young, Ian S. [1 ]
McKibben, Bronac [1 ]
McEneny, Jane [1 ]
机构
[1] Queens Univ Belfast, Ctr Clin & Populat Sci, Nutr & Metab Grp, Belfast, Antrim, North Ireland
关键词
apolipoproteins; cholesteryl ester transfer protein; lecithin : cholesterol acyltransferase; lipid hydroperoxides; single radial immunodiffusion; transferrin; ultracentrifugation;
D O I
10.1194/jlr.M600094-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The plasma HDLs represent a major class of cholesterol-transporting lipoprotein that can be divided into two distinct subfractions, HDL2 and HDL3, 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.
引用
收藏
页码:86 / 95
页数:10
相关论文
共 50 条
[11]  
CHAPMAN MJ, 1981, J LIPID RES, V22, P339
[12]  
CHEUNG MC, 1979, J LIPID RES, V20, P200
[13]  
CHUNG BH, 1986, METHOD ENZYMOL, V128, P181
[14]  
CHUNG BH, 1980, J LIPID RES, V21, P284
[15]   High-density lipoproteins differentially modulate cytokine-induced expression of E-selectin and cyclooxygenase-2 [J].
Cockerill, GW ;
Saklatvala, J ;
Ridley, SH ;
Yarwood, H ;
Miller, NE ;
Oral, B ;
Nithyanathan, S ;
Taylor, G ;
Haskard, DO .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (04) :910-917
[16]   Inactivation of cholesteryl ester transfer protein by cysteine modification [J].
Connolly, DT ;
Heuvelman, D ;
Glenn, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 223 (01) :42-47
[17]  
DELALLA OF, 1954, METHOD BIOCHEM ANAL, V1, P459
[18]  
DIAS VC, 1988, CLIN CHEM, V34, P2322
[19]  
DURRINGTON PN, 1995, HYPERLIPIDAEMIA DIAG
[20]  
EISENBERG S, 1984, J LIPID RES, V25, P1017