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PMID: 9323590 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Cholesterol efflux mediated by apolipoproteins is an active cellular process distinct from efflux mediated by passive diffusion.

Journal of lipid research ·Vol. 38 ·No. 9 ·1997-09-00 ·Pages 1807-21

Mendez AJ

Abstract

It is becoming increasingly accepted that removal of cellular cholesterol occurs by at least two pathways, one involving the well-described aqueous diffusion mechanism and another promoted by lipid-free apolipoproteins. We compared the contribution of apolipoprotein-dependent and -independent pathways, taking into consideration the influence of cellular metabolism, on cholesterol efflux promoted by different extracellular acceptor types. The acceptors used were assumed to participate in only passive efflux by lipid-dependent mechanisms (phospholipid vesicles and trypsin-modified high density lipoproteins) or to stimulate efflux by apolipoprotein-dependent pathways (purified apolipoprotein A-I and high density lipoproteins). Apolipoprotein-mediated cholesterol efflux was only apparent in growth-arrested or cholesterol-enriched cells and required metabolic energy. In contrast, cholesterol efflux by apolipoprotein-depleted acceptors did not depend on cell growth state, cholesterol enrichment, or metabolic energy. Apolipoprotein-mediated efflux was not observed at temperatures below 22 degrees C, while apolipoprotein-independent efflux was only reduced by 50% at 4 degrees C compared with incubations at 37 degrees C. Additionally, apolipoproteins promoted a more rapid and larger decrease in intracellular cholesteryl esters when measured by changes in cholesteryl ester radioactivity, mass, or the pool of cholesterol available for esterification by acyl coenzyme A:cholesterol acyltransferase. Efflux of excess cellular cholesterol by an apolipoprotein-dependent pathway appears to involve specific cellular events consistent with the properties of an active transport pathway and distinguishable from cholesterol efflux by apolipoprotein-depleted acceptors through passive mechanisms.

MeSH Terms
Apolipoprotein A-I/metabolism Apolipoproteins/metabolism Biological Transport/drug effects Biological Transport, Active/drug effects Cell Division Cells, Cultured Cholesterol/metabolism Cholesterol Esters/metabolism Diffusion Energy Metabolism/drug effects Esterification Humans Kinetics Lipoproteins, HDL/metabolism Potassium Cyanide/toxicity Tangier Disease/metabolism Temperature
Chemicals
Apolipoprotein A-I Apolipoproteins Cholesterol Esters Lipoproteins, HDL Cholesterol Potassium Cyanide
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Mendez A J
University of Miami School of Medicine, Diabetes Research Institute, Miami, FL 33101, USA.
Article Info
Journal
Journal of lipid research
Abbr.
J Lipid Res
ISSN
0022-2275
Published
1997-09-00
Pages
1807-21
Language
English
Region
United States
NLM ID
0376606
Subset
IM
Grants
NHLBI NIH HHS · HL53451 · United States
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