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Journal of Lipid Research, Vol 37, 2510-2524, Copyright © 1996 by Lipid Research, Inc.
AJ Mendez and L Uint
Several studies have demonstrated that lipid-free apolipoproteins can
promote cholesterol and phospholipid efflux from cells; however, the
mechanisms and the role of cell-mediated pathways involved remain
incompletely elucidated. We have recently demonstrated that brefeldin A or
monensin, agents that disrupt Golgi apparatus structure and function,
inhibit intracellular cholesterol efflux from cells to high density
lipoproteins. In the present study we examined the effects of those agents
on cell cholesterol and phospholipid efflux to purified apolipoprotein A-I
(apoA-I) and apolipoprotein-depleted acceptors from cholesterol-loaded
fibroblasts. Brefeldin A or monensin treatment of cells during incubation
with apoA-I inhibited efflux of cellular cholesterol by greater than 80%
compared with control cells, measured by changes in cellular cholesterol
radioactivity, mass, and the substrate pool of cholesterol available for
esterification by acyl coenzyme A:cholesterol acyltransferase. Inhibition
of cholesterol efflux by these agents could not be overcome by increasing
the apoA-I concentration and persisted during incubations up to 24 h.
Similarly, brefeldin A and monensin inhibited up to 80% of apoA-I-mediated
efflux of labeled phospholipids from cholesterol-loaded cells relative to
controls. In contrast, lipid efflux mediated by apolipoprotein-depleted
acceptors (trypsin-modified HDL and sonicated phospholipid vesicles) was
not sensitive to these drugs. On the basis the known effects of brefeldin A
and monensin on Golgi apparatus structure and function, these results are
consistent with the notion that efflux of cell lipids by
apolipoprotein-dependent mechanisms, but not by apolipoprotein- independent
mechanisms, require active cellular processes involving an intact and
functional Golgi apparatus.
ARTICLES
Apolipoprotein-mediated cellular cholesterol and phospholipid efflux depend on a functional Golgi apparatus
Cardiac Unit (GRJ-1422), Massachusetts General Hospital, Boston 02114, USA.
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