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Journal of Lipid Research, Vol. 43, 2037-2041, December 2002
Copyright © 2002 by Lipid Research, Inc.
Rapid Communication |

* Departments of Biological Chemistry and Medicine, University of California, Los Angeles, CA 90095
Molecular Biology Institute, University of California, Los Angeles, CA 90095
1 To whom correspondence should be addressed. e-mail: pedwards{at}mednet.ucla.edu
ABSTRACT
Affymetrix microarray data and Northern blot assays demonstrated that phospholipid transfer protein (PLTP) was induced 6-fold when either murine or human macrophages were incubated in the presence of ligands for the liver X receptor (LXR) and the retinoid X receptor. Two functional LXR response elements (LXREs) were identified and characterized in the proximal promoter of the human PLTP gene. One LXRE corresponds to a traditional direct repeat separated by 4 bp. However, the second LXRE is novel in that it corresponds to an inverted repeat separated by 1 bp, and is identical to the farnesoid X receptor response element. These studies demonstrate that PLTP is a direct target for activated LXR and farnesoid X receptor (FXR). In addition, apolipoprotein E (apoE), a known LXR target gene in macrophages, was shown to be activated in liver cells by FXR ligands.
Taken together, the current data suggest that a small number of genes that currently include PLTP, apoE, and apoC-II, are induced in macrophages by activated LXR and in liver by activated FXR.
Abbreviations: apo, apolipoprotein; CDCA, chenodeoxycholic acid; EMSA, electrophoretic mobility shift assay; FXR, farnesoid X receptor; FXRE, FXR response element; GW, GW4064, a synthetic FXR agonist; LG, LG100153, a synthetic RXR agonist; LXR, liver X receptor; LXRE, LXR response element; RXR, retinoid X receptor
Supplementary key words macrophages foam cells hepatocytes phospholipid transfer protein liver X receptor retinoid X receptor
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