Mechanism of cholesterol efflux in humans after infusion of reconstituted high-density lipoprotein

Anh Hoang, Brian G. Drew, Hann Low, Alan T. Remaley, Paul John Nestel, Bronwyn A. Kingwell, Dmitri Sviridov

Research output: Contribution to journalArticleResearchpeer-review

56 Citations (Scopus)

Abstract

Objectives Infusion of reconstituted HDL (rHDL) leads to changes in HDL metabolism as well as to an increased capacity of plasma to support cholesterol efflux providing an opportunity to investigate mechanisms linking cholesterol efflux to changes in plasma HDL. Methods and results Patient plasmas after infusion of rHDL were tested ex vivo for their capacity to stimulate cholesterol efflux. Reconstituted HDL enhanced mobilization of cholesterol from tissues in vivo as shown by rising HDL cholesterol concentrations over the infusion period. Infusion of rHDL in vivo led to increased cholesterol efflux ex vivo; surprisingly, removing apoB-containing lipoproteins while preserving all HDL subfractions eliminated this increase. Infusion of rHDL led to the remodelling of plasma HDL; however, the capacity of plasma to support cholesterol efflux did not correlate with changes in the concentrations of any of HDL subfractions. Unmodified rHDL accounted for only a proportion of the increment in cholesterol efflux capacity. Furthermore, studies using HeLa and BHK cells overexpressing ABCA1, ABCG1, and SR-B1 showed that the contribution of these cellular mediators of cholesterol efflux to the enhanced capacity of plasma for the efflux was minimal. Conclusion Enhanced cholesterol efflux from tissues requires the presence of apoB-containing lipoproteins and may involve enhanced flow of cholesterol through multiple components of the reverse cholesterol transport pathway rather than being determined by a specific HDL subfraction.

Original languageEnglish
Pages (from-to)657-665
Number of pages9
JournalEuropean Heart Journal
Volume33
Issue number5
DOIs
Publication statusPublished - Mar 2012
Externally publishedYes

Keywords

  • Cholesterol
  • Lipids
  • Lipoproteins

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