15-Lipoxygenase-mediated modification of high-density lipoproteins impairs SR-BI- and ABCA1-dependent cholesterol efflux from macrophages

Biochim Biophys Acta. 2006 Mar;1761(3):292-300. doi: 10.1016/j.bbalip.2006.03.009. Epub 2006 Apr 7.

Abstract

Elevated plasma levels of high-density lipoprotein cholesterol (HDL-C) are atheroprotective and HDL-dependent reverse cholesterol transport has been related to this effect. HDL particles may, however, undergo modifications that affect their biological activities. Lipoxygenases (LOs) belong to a family of lipid peroxidizing enzymes; among them, reticulocyte-type 15-lipoxygenase (15-LO-1) appears to play a pathophysiological role in atherosclerosis, as its expression is increased in atherosclerotic plaques and it has been shown to oxidize low-density lipoproteins to an atherogenic form. In this work we investigated the impact of in vitro 15-lipoxygenase-catalyzed modification of HDL3 on their ability to act as cholesterol acceptor and found that 15-LO-modified HDL3 were less effective in mediating cholesterol efflux from lipid-laden J774 cells. A reduced binding of 15-LO-modified HDL3 to scavenger receptor class B, type I (SR-BI), due to HDL apoproteins cross-linking, explained, at least in part, the observed reduction of cholesterol efflux. In addition, ATP-binding cassette transporter A1 (ABCA1)-mediated cholesterol efflux was also reduced, as a consequence of pre-beta-particles loss after HDL3 modification. These results suggest that 15-lipoxygenase might induce structural alterations of HDL3 particles that impair their capability of triggering reverse cholesterol transport.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter 1
  • ATP-Binding Cassette Transporters / metabolism*
  • Animals
  • Arachidonate 15-Lipoxygenase / metabolism*
  • Cell Line
  • Cholesterol / analogs & derivatives
  • Cholesterol / metabolism*
  • Humans
  • Lipoproteins, HDL / metabolism*
  • Macrophages / cytology
  • Macrophages / metabolism*
  • Mice
  • Rabbits
  • Scavenger Receptors, Class B / metabolism*
  • Thiobarbituric Acid Reactive Substances / metabolism

Substances

  • ABCA1 protein, human
  • ATP Binding Cassette Transporter 1
  • ATP-Binding Cassette Transporters
  • Lipoproteins, HDL
  • Scarb1 protein, mouse
  • Scavenger Receptors, Class B
  • Thiobarbituric Acid Reactive Substances
  • cholesteryl oleyl ether
  • Cholesterol
  • Arachidonate 15-Lipoxygenase