Abstract

ATP-binding cassette protein A1 (ABCA1) is a cholesterol transporter that contributes to the active transport/removal of excess cellular cholesterol. ABCA1 expression is up-regulated when cells accumulate cholesterol.AimsThe purpose of this study was to determine any correlation between extracellular phospholipid levels and ABCA1 expression and function.MethodologyHuman foreskin fibroblasts were incubated with cholesterol alone or cholesterol and phosphatidylcholine. Total RNA was isolated and subjected to end-point RT-PCR to compare ABCA1 transcript levels. Cell lysates were subjected to Western blot analysis to compare ABCA1 protein levels. Cells were loaded with radiolabeled cholesterol and cellular cholesterol efflux was measured in the presence and absence of apoE, a cholesterol acceptor. ApoE-dependent efflux was calculated as a measure of ABCA1-mediated efflux.ResultsHere we show that incubation of cholesterol-loaded human skin fibroblasts with L-α-phosphatidylcholine (PC) decreases ABCA1 mRNA and protein levels by 93% and 57%, respectively, compared to cells loaded with cholesterol alone. Similarly, PC treatment results in a 25% reduction in ABCG1 mRNA levels compared to cells treated with cholesterol alone, but there is no change in SR-BI transcript levels. Subsequent incubation of phospholipid-treated cells with a cholesterol acceptor such as apoE for 24 hours shows a 65% reduction in ABCA1-mediated cholesterol efflux compared to efflux in cells not treated with PC. During the lipid treatment itself, there is a 2.7-fold greater loss of cholesterol from PC treated cells compared to cells treated with cholesterol alone. Measurement of cholesterol in cellular lipid extracts reveals that cells incubated in the presence of phosphatidylcholine are significantly depleted of cholesterol having only 20% of the cholesterol compared to cells loaded with cholesterol alone.ConclusionThus, phosphatidylcholine facilitates removal of cellular cholesterol, thereby negating the cholesterol-dependent induction of ABCA1 message, protein and function.

Highlights

  • The adenosine triphosphate binding cassette protein A1 (ABCA1) is a cholesterol transporter responsible for the removal of free cholesterol and phospholipids from cells

  • Here we show that incubation of cholesterol-loaded human skin fibroblasts with L-αphosphatidylcholine (PC) decreases ABCA1 mRNA and protein levels by 93% and 57%, respectively, compared to cells loaded with cholesterol alone

  • Subsequent incubation of phospholipid-treated cells with a cholesterol acceptor such as apoE for 24 hours shows a 65% reduction in ABCA1-mediated cholesterol efflux compared to efflux in cells not treated with PC

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Summary

Introduction

The adenosine triphosphate binding cassette protein A1 (ABCA1) is a cholesterol transporter responsible for the removal of free cholesterol and phospholipids from cells. The resulting flow of cholesterol from peripheral tissues to the liver is termed reverse cholesterol transport (RCT), and influences the plasma lipoprotein profile, HDL levels [1,2]. Mutations in the ABCA1 gene are associated with familial hypoalphalipoproteinemia and a higher incidence of cardiovascular disease. The lipidation of free apoA-I results in the formation of discoidal pre-beta-migrating HDL particles. The newly acquired cholesterol is esterified by the HDL-associated enzyme lecithin: cholesterol acyltransferase (LCAT) transforming the particle into spherical mature HDL, which carries cholesterol to the liver for degradation [4,5]

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