Abstract

Our aim in this study was to investigate the effect of aging on the capacity of HDLs to promote reverse cholesterol transport. HDLs were isolated from plasma of young (Y-HDL) and elderly (E-HDL) subjects. HDL-mediated cholesterol efflux was studied using THP-1 and J774 macrophages. Our results show that E-HDLs present a lower capacity to promote cholesterol efflux than Y-HDLs (41.7 +/- 1.4% vs. 49.0 +/- 2.2%, respectively; P = 0.013). Reduction in the HDL-mediated cholesterol efflux capacity with aging was more significant with HDL(3) than HDL(2) (Y-HDL(3), 57.3 +/- 1% vs. E-HDL(3), 50.9 +/- 2%; P = 0.012). Moreover, our results show that ABCA1-mediated cholesterol efflux is the more affected pathway in terms of cholesterol-removing capacity. Interestingly, the composition and structure of HDL revealed a reduction in the phosphatidylcholine-sphingomyelin ratio (E-HDL, 32.7 +/- 2.7 vs. Y-HDL, 40.0 +/- 1.9; P = 0.029) and in the phospholipidic layer membrane fluidity in E-HDL compared with Y-HDL as well as an alteration in the apolipoprotein A-I structure and charge. In conclusion, our results shown that E-HDLs present a reduced capacity to promote cholesterol efflux, principally through the ABCA1 pathway, and this may explain the increase of the incidence of cardiovascular diseases observed during aging.

Highlights

  • Our aim in this study was to investigate the effect of aging on the capacity of HDLs to promote reverse cholesterol transport

  • The concept of reverse cholesterol transport (RCT), as suggested by Glomset [7], consists of the movement of cholesterol from the peripheral tissues to the liver, which starts by the efflux of free cholesterol (FC) and phospholipids from cells of peripheral tissues to preb-migrating lipid-poor or lipid-free apolipoprotein A-I and to HDL3 [7,8,9]

  • To examine the effect of aging on the antiatherogenic activities of HDL and their ability to promote RCT, we assessed the capacity of HDL obtained from young (Y-HDL) and elderly (E-HDL) healthy subjects to enable cholesterol efflux

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Summary

Introduction

Our aim in this study was to investigate the effect of aging on the capacity of HDLs to promote reverse cholesterol transport. Our results shown that E-HDLs present a reduced capacity to promote cholesterol efflux, principally through the ABCA1 pathway, and this may explain the increase of the incidence of cardiovascular diseases observed during aging.—Berrougui, H., M. It was shown that another transporter, ABCG1, promotes mass cholesterol efflux from cells to mature HDL particles (HDL2 and HDL3) but not to lipid-poor apoA-I [5,6]. Both ABCA1 and ABCG1 are abundant in macrophages, especially after cholesterol loading, suggesting their importance for the cholesterol efflux process. This article is available online at http://www.jlr.org

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