PT  - JOURNAL ARTICLE
AU  - Paul B. Noto
AU  - Yuri Bukhtiyarov
AU  - Meng Shi
AU  - Brian M. McKeever
AU  - Gerard M. McGeehan
AU  - Deepak S. Lala
TI  - Regulation of Sphingomyelin Phosphodiesterase Acid-Like 3A Gene (<em>SMPDL3A</em>) by Liver X Receptors
AID  - 10.1124/mol.112.078865
DP  - 2012 Oct 01
TA  - Molecular Pharmacology
PG  - 719--727
VI  - 82
IP  - 4
4099  - http://molpharm.aspetjournals.org/content/82/4/719.short
4100  - http://molpharm.aspetjournals.org/content/82/4/719.full
SO  - Mol Pharmacol2012 Oct 01; 82
AB  - Liver X receptor (LXR) α and LXRβ function as physiological sensors of cholesterol metabolites (oxysterols), regulating key genes involved in cholesterol and lipid metabolism. LXRs have been extensively studied in both human and rodent cell systems, revealing their potential therapeutic value in the contexts of atherosclerosis and inflammatory diseases. The LXR genome landscape has been investigated in murine macrophages but not in human THP-1 cells, which represent one of the frequently used monocyte/macrophage cell systems to study immune responses. We used a whole-genome screen to detect direct LXR target genes in THP-1 cells treated with two widely used LXR ligands [N-(2,2,2-trifluoroethyl)-N-[4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)-ethyl]phenyl]-benzenesulfonamide (T0901317) and 3-[3-[N-(2-chloro-3-trifluoromethylbenzyl)-(2,2-diphenylethyl)amino]propyloxy] phenylacetic acid hydrochloride (GW3965)]. This screen identified the sphingomyelin phosphodiesterase acid-like 3A (SMPDL3A) gene as a novel LXR-regulated gene, with an LXR response element within its promoter. We investigated the regulation of SMPDL3A gene expression by LXRs across several human and mouse cell types. These studies indicate that the induction of SMPDL3A is LXR-dependent and is restricted to human blood cells with no induction observed in mouse cellular systems.