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Journal of Lipid Research, Vol 26, 487-494, Copyright © 1985 by Lipid Research, Inc.
S Eisenberg
The effect of lipid transfer proteins on the exchange and transfer of
cholesteryl esters from rat plasma HDL2 to human very low (VLDL) and low
density (LDL) lipoprotein populations was studied. The use of a combination
of radiochemical and chemical methods allowed separate assessment of
[3H]cholesteryl ester exchange and of cholesteryl ester transfer. VLDL-I
was the preferred acceptor for transferred cholesteryl esters, followed by
VLDL-II and VLDL-III. LDL did not acquire cholesteryl esters. The
contribution of exchange of [3H]cholesteryl esters to total transfer was
highest for LDL and decreased in reverse order along the VLDL density
range. Inactivation of lecithin: cholesterol acyltransferase (LCAT) and
heating the HDL2 for 60 min at 56 degrees C accelerated transfer and
exchange of [3H]cholesteryl esters. Addition of lipid transfer proteins
increased cholesterol esterification in all systems. The data demonstrate
that large-sized, triglyceride-rich VLDL particles are preferred acceptors
for transferred cholesteryl esters. It is suggested that enrichment of very
low density lipoproteins with cholesteryl esters reflects the triglyceride
content of the particles.
ARTICLES
Preferential enrichment of large-sized very low density lipoprotein populations with transferred cholesteryl esters
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