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Journal of Lipid Research, Vol 37, 1579-1590, Copyright © 1996 by Lipid Research, Inc.
D Masson, A Athias and L Lagrost
Plasma high density lipoprotein-3 (HDL3) subfractions with different
composition and electric charge properties were isolated by anion exchange
chromatography; their ability to exchange cholesteryl esters with low
density lipoproteins (LDL) in the presence of the human cholesteryl ester
transfer protein (CETP) was studied. The rate of radiolabeled cholesteryl
esters transferred between LDL and HDL3 was progressively enhanced as the
negative charge density of HDL3 particles increased, until the maximal
transfer value was reached with a charge density ranging between -2,200 and
-2,250 esu/cm2. Consistent data were obtained when cholesteryl ester
transfer was measured either from radiolabeled LDL towards HDL3 or from
radiolabeled HDL3 towards LDL. In both cases, a progressive decrease in the
cholesteryl ester transfer rate was observed as the charge density
increased above the optimal value. When HDL3 particles were progressively
enriched with apoA-II with no modification of their lipid content, the
electronegative charge progressively decreased. In good agreement with data
obtained with native HDL3 subfractions isolated from human plasma, the rate
of radiolabeled cholesteryl esters transferred from LDL towards apoA-II-
enriched HDL3 increased progressively as the density of negative charge
increased, until an optimal surface charge density of approx. -2,200
esu/cm2, was reached. As the charge density of apoA-II-enriched HDL3
exceeded the optimal value, the cholesteryl ester transfer rate was
substantially reduced. Consistent observations were made by substituting
apoA-II for apoA-I either in immunopurified HDL3 particles containing
mainly apoA-I or in the plasma HDL3 subfractions with the highest
electronegativity. It is concluded that the charge density of plasma HDL3
constitutes one major determinant of maximal CETP activity.
ARTICLES
Evidence for electronegativity of plasma high density lipoprotein-3 as one major determinant of human cholesteryl ester transfer protein activity
Laboratoire de Biochimie des Lipoproteines, INSERM CJF 93-10, Faculte de Medecine, France.
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