Impact of LDL apheresis on atheroprotective reverse cholesterol transport pathway in familial hypercholesterolemia

• Published in: Journal of lipid research Vol. 53; no. 4; pp. 767 - 775
• Main Authors: Orsoni, Alexina, Villard, Elise F., Bruckert, Eric, Robillard, Paul, Carrie, Alain, Bonnefont-Rousselot, Dominique, Chapman, M. John, Dallinga-Thie, Geesje M., Le Goff, Wilfried, Guerin, Maryse
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.04.2012; American Society for Biochemistry and Molecular Biology; The American Society for Biochemistry and Molecular Biology; Elsevier
• Subjects: Adult; Animals; Apolipoproteins B - genetics; Apolipoproteins B - metabolism; ATP Binding Cassette Transporter, Subfamily G, Member 1; ATP-Binding Cassette Transporters - genetics; ATP-Binding Cassette Transporters - metabolism; Biological Transport; Blood Component Removal - methods; cellular cholesterol efflux; CHO Cells; Cholesterol Ester Transfer Proteins - genetics; Cholesterol Ester Transfer Proteins - metabolism; Cholesterol Esters - metabolism; Cholesterol, HDL - metabolism; Cholesterol, LDL - isolation & purification; cholesteryl ester transfer protein; Cricetinae; Esterification; Female; high density lipoprotein; high density lipoprotein cholesteryl ester uptake; High-Density Lipoproteins, Pre-beta - genetics; High-Density Lipoproteins, Pre-beta - metabolism; Humans; Hyperlipoproteinemia Type II - genetics; Hyperlipoproteinemia Type II - metabolism; Hyperlipoproteinemia Type II - pathology; Hyperlipoproteinemia Type II - therapy; Life Sciences; Lipid Metabolism; low density lipoprotein; Macrophages - metabolism; Male; Mice; Middle Aged; Scavenger Receptors, Class B - genetics; Scavenger Receptors, Class B - metabolism; Young Adult; low density lipoprotein; high density lipoprotein cholesteryl ester uptake; cellular cholesterol efflux; high density lipoprotein; cholesteryl ester transfer protein
• ISSN: 0022-2275; 1539-7262
• DOI: 10.1194/jlr.M024141

In familial hypercholesterolemia (FH), low HDL cholesterol (HDL-C) levels are associated with functional alterations of HDL particles that reduce their capacity to mediate the reverse cholesterol transport (RCT) pathway. The objective of this study was to evaluate the consequences of LDL apheresis on the efficacy of the RCT pathway in FH patients. LDL apheresis markedly reduced abnormal accelerated cholesteryl ester transfer protein (CETP)-mediated cholesteryl ester (CE) transfer from HDL to LDL, thus reducing their CE content. Equally, we observed a major decrease (−53%; P < 0.0001) in pre-β1-HDL levels. The capacity of whole plasma to mediate free cholesterol efflux from human macrophages was reduced (−15%; P < 0.02) following LDL apheresis. Such reduction resulted from a marked decrease in the ABCA1-dependent efflux (−71%; P < 0.0001) in the scavenger receptor class B type I-dependent efflux (−21%; P < 0.0001) and in the ABCG1-dependent pathway (−15%; P < 0.04). However, HDL particles isolated from FH patients before and after LDL apheresis displayed a similar capacity to mediate cellular free cholesterol efflux or to deliver CE to hepatic cells. We demonstrate that rapid removal of circulating lipoprotein particles by LDL apheresis transitorily reduces RCT. However, LDL apheresis is without impact on the intrinsic ability of HDL particles to promote either cellular free cholesterol efflux from macrophages or to deliver CE to hepatic cells.