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Journal of Lipid Research, Vol 36, 2630-2638, Copyright © 1995 by Lipid Research, Inc.
R Kraemer, KB Pomerantz, S Kesav, TJ Scallen and DP Hajjar
Cholesterol enrichment of vascular smooth muscle cells, as occurs under
conditions of hypercholesterolemia and atherosclerosis, is accompanied by
specific changes in cholesterol metabolism and in intracellular cholesterol
trafficking. Sterol-carrier protein-2 (SCP2), an intracellular lipid
binding protein, enhances the activation of enzymes involved in cholesterol
metabolism. It may also enhance cholesterol efflux by regulating the size
of the "fast" cholesterol pool available for efflux to high density
lipoproteins. However, a definitive role for SCP2 in arterial cholesterol
metabolism is unclear. Therefore, we examined the expression of SCP2 (13.1
kD), SCPx (58 kD), and p30 (30.8 kD) in cultured arterial smooth muscle
cells under conditions of cholesterol enrichment. We found that SCP2, SCPx,
and p30 are localized principally in the cytosolic fraction, with lesser
amounts associated with the nuclear/peroxisomal fraction; the expression of
SCP2 protein and mRNA, but not SCPx, is increased after exposure of smooth
muscle cells to cationized LDL. In contrast to the increased expression of
SCP2, the expression of p30 decreases after cholesterol enrichment of
smooth muscle cells. Coupled with previous studies demonstrating enhanced
cholesterol efflux from cholesterol-enriched smooth muscle cells in
response to high density lipoproteins, our results suggest that increased
expression of SCP2 may partly mediate the cholesterol trafficking process.
ARTICLES
Cholesterol enrichment enhances expression of sterol-carrier protein-2: implications for its function in intracellular cholesterol trafficking
Department of Biochemistry, Cornell University Medical College, New York, NY 10021, USA.
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