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A more recent version of this article appeared on July 1, 2005
Originally published In Press as doi:10.1194/jlr.M400477-JLR200 on May 31, 2005
Papers In Press, published online ahead of print January 16, 2005
J. Lipid Res., doi:10.1194/jlr.M400477-JLR200
Submitted on December 6, 2004
Revised on January 1, 1998
Accepted on January 16, 2005
Structural modification of plasma HDL by phospholipids promotes efficient ABCA1-mediated cholesterol release
Houssein Hajj Hassan, Sacha Blain, Betsie Boucher, Maxime Denis, Larbi Krimbou, and Jacques Genest
Cardiology Dept., McGill University Health Center, Montreal, QC H3A 1A1
Corresponding Author: jacques.genest{at}muhc.mcgill.ca
It has been suggested that ABCA1 interacts preferentially with lipid-poor apoA-I. Here, we show that treatment of plasma with dimyristoyl phosphatidylcholine multilamellar vesicles (DMPC-MLV) generates pre-<IMG SRC="/math/beta.gif" ALIGN="BASELINE" ALT="beta "><IMG SRC="/math/sub.gif" ALIGN="BASELINE" ALT="sub ">1-LpA-I-like particles similar to those of native plasma. Isolated pre-<IMG SRC="/math/beta.gif" ALIGN="BASELINE" ALT="beta "><IMG SRC="/math/sub.gif" ALIGN="BASELINE" ALT="sub ">1-LpA-I-like particles inhibited the binding of <SUP>r</SUP>125I-apoA-I to ABCA1 more efficiently than HDL <IMG SRC="/math/sub.gif" ALIGN="BASELINE" ALT="sub ">3 (IC50 = 2.20 ± 0.35 vs. 37.60 ± 4.78 µg/mL). We next investigated the ability of pre-<IMG SRC="/math/beta.gif" ALIGN="BASELINE" ALT="beta "><IMG SRC="/math/sub.gif" ALIGN="BASELINE" ALT="sub ">1-LpA-I-like particles to promote cholesterol efflux from J774 macrophages stimulated or not with cAMP. DMPC enrichment of plasma promoted cholesterol efflux from either stimulated or unstimulated cells in a dose-dependent manner. Comparison of maximal efflux (Vmax efflux) and the DMPC concentration that elicited half maximal efflux (EC50 efflux) between unstimulated and stimulated cells after a 4-hour incubation showed that Vmax efflux is significantly higher for stimulated cells (11.8 ± 1.2 % vs. 8.7 ± 0.5 %), whereas the value of EC50 efflux is higher for unstimulated cells (610 ± 89 vs. 136 ± 16 µM DMPC). Furthermore, cholesterol efflux to DMPC-treated plasma was reduced by 30% in the presence of glyburide. Finally, treatment of Tangier disease (TD) plasma with DMPC affected neither the amount of pre-<IMG SRC="/math/beta.gif" ALIGN="BASELINE" ALT="beta ">-HDL nor cholesterol efflux. These results indicate that DMPC enrichment of normal plasma resulted in redistribution of apoA-I from <IMG SRC="/math/alpha.gif" ALIGN="BASELINE" ALT="alpha ">-HDL to pre-<IMG SRC="/math/beta.gif" ALIGN="BASELINE" ALT="beta ">-HDL, allowing for more efficient ABCA1-mediated cholesterol release. Increasing plasma pre-<IMG SRC="/math/beta.gif" ALIGN="BASELINE" ALT="beta "><IMG SRC="/math/sub.gif" ALIGN="BASELINE" ALT="sub ">1-LpA-I level by either pharmacological agents or direct infusions might prevent foam cell formation and reduce atherosclerotic vascular disease.

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Copyright © 2005 by the American Society for Biochemistry and Molecular Biology.
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