Abstract

Cholesteryl ester transfer protein (CETP) is a key protein involved in the reverse cholesterol transport pathway. The regulation of CETP by dietary fats is not clearly understood. Transgenic mice expressing human CETP under the control of its natural flanking region were fed low- or high-fat diets enriched in monounsaturated fatty acids (MUFAs) or saturated fatty acids in the presence or absence of cholesterol. Addition of cholesterol to the low-fat MUFA diet increased CETP activity and mRNA expression, whereas addition of cholesterol to the high-fat MUFA diet led to a decrease in CETP activity and mRNA expression. In SW 872 cells, oleic acid and cholesterol stimulated CETP gene expression when given alone. However, addition of fatty acids along with cholesterol interfered with the stimulatory effect of cholesterol on CETP gene regulation. Cholesterol-mediated stimulation of CETP involves the transcription factor liver X receptor alpha (LXRalpha). High-fat MUFA diets inhibited the expression of LXRalpha, and addition of cholesterol to the high-fat MUFA diet did not rescue LXRalpha expression. Therefore, we present evidence for the first time that inhibition of LXRalpha expression by a high-fat MUFA diet leads to inhibition of CETP stimulation by cholesterol.

Highlights

  • Cholesteryl ester transfer protein (CETP) is a key protein involved in the reverse cholesterol transport pathway

  • We further investigated whether the quantity and quality of dietary fats alter the expression of liver X receptor (LXR)␣, which in turn might modulate the regulatory potential of cholesterol on CETP expression

  • Feeding a high-fat diet enriched in monounsaturated fatty acids (MUFAs) or saturated fatty acid (SFA) had no significant effect on plasma total cholesterol concentrations compared with feeding a low-fat MUFA or MUFA ϩ cholesterol

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Summary

Introduction

Cholesteryl ester transfer protein (CETP) is a key protein involved in the reverse cholesterol transport pathway. 2356 Journal of Lipid Research Volume 46, 2005 with alterations in CETP levels, show that an absence of CETP is associated with the disruption of cholesterol efflux from cell membranes, of cholesterol esterification, and of cholesteryl ester transfer to apolipoprotein B-containing lipoproteins [1]. These disruptions impair cholesterol movement to the liver; a high CETP activity might be antiatherogenic as it removes excess cholesterol from the arterial wall.

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