The Role of Liver X Receptor-α in the Fatty Acid Regulation of Hepatic Gene Expression

Anjali Pawar, Daniela Botolin, David J. Mangelsdorf, Donald B. Jump

Research output: Contribution to journalArticle

118 Citations (Scopus)

Abstract

Liver X receptors (LXR) α and β play an important role in regulating the expression of genes involved in hepatic bile and fatty acid synthesis, glucose metabolism, as well as sterol efflux. Studies with human embryonic kidney 293 cells indicate that unsaturated fatty acids interfere with oxysterols binding to LXR and antagonize oxysterol-induced LXRα activity. In this report, we evaluated the effects of unsaturated fatty acids on LXR-regulated hepatic gene expression. The LXR agonist, T1317, induced mRNAs encoding sterol regulatory element-binding protein 1c (SREBP-1c) and two SREBP-1c-regulated lipogenic genes, e.g. fatty-acid synthase and the S14 protein in primary hepatocytes. Treatment of hepatocytes with eicosapentaenoic acid (20:5n-3) suppressed these mRNAs in the absence and presence of T1317. The cis-regulatory elements targeted by T1317 were not required for fatty-acid suppression of FAS or S14 promoter activity. In contrast to SREBP-1-regulated lipogenic genes, 20:5n-3 had no effect on the T1317 induction of ABCG5 or ABCG8 in the rat hepatoma cell line, FTO-2B. These two genes require LXR but not SREBP-1c for their expression. Feeding rats a diet supplemented with fish oil suppressed hepatic SREBP-1c-regulated genes and induced PPARα-regulated genes but had no effect on the LXR-regulated transcripts, CYP7A1, ABCG5, or ABCG8. Transfection studies, using either full-length hLXRα or a chimera containing only the LXRα ligand binding domain, indicate that a wide array of unsaturated fatty acids had little effect on LXRα activity in primary hepatocytes or FTO-2B. These studies suggest that LXRα is not a target for unsaturated fatty acid regulation in primary rat hepatocytes or in liver. Thus, oxysterol/LXR-mediated regulation of transcripts involved in bile acid synthesis or sterol efflux appear insensitive to dietary unsaturated fatty acids. The unsaturated fatty acid suppression of SREBP-1 and its targeted lipogenic genes is independent of LXRα.

Original languageEnglish (US)
Pages (from-to)40736-40743
Number of pages8
JournalJournal of Biological Chemistry
Volume278
Issue number42
DOIs
StatePublished - Oct 17 2003

Fingerprint

Gene Expression Regulation
Gene expression
Liver
Fatty Acids
Unsaturated Fatty Acids
Sterol Regulatory Element Binding Protein 1
Genes
Hepatocytes
Rats
Sterols
Bile Acids and Salts
Liver X Receptors
Gene Expression
Fatty Acid Synthases
Messenger RNA
Peroxisome Proliferator-Activated Receptors
Eicosapentaenoic Acid
Fish Oils
Nutrition
Metabolism

ASJC Scopus subject areas

  • Biochemistry

Cite this

The Role of Liver X Receptor-α in the Fatty Acid Regulation of Hepatic Gene Expression. / Pawar, Anjali; Botolin, Daniela; Mangelsdorf, David J.; Jump, Donald B.

In: Journal of Biological Chemistry, Vol. 278, No. 42, 17.10.2003, p. 40736-40743.

Research output: Contribution to journalArticle

Pawar, Anjali ; Botolin, Daniela ; Mangelsdorf, David J. ; Jump, Donald B. / The Role of Liver X Receptor-α in the Fatty Acid Regulation of Hepatic Gene Expression. In: Journal of Biological Chemistry. 2003 ; Vol. 278, No. 42. pp. 40736-40743.
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