Abstract
Liver X receptors (LXRα and LXRβ) are members of the nuclear receptor superfamily and are activated by oxysterols and intermediates in the cholesterol synthetic pathway. The pivotal role of LXRs in the metabolic conversion of cholesterol to bile acids is well established. Analysis of gene expression in LXRα and LXRβ deficient mice have confirmed that LXR regulates a number of target genes involved in both cholesterol and fatty acid metabolism in liver, macrophages and intestine. The observation that LXRα is responsive to fatty acids and is expressed in metabolic tissues suggests that it also plays a general role in lipid metabolism. Adipose tissue is the main storage site for fat in the body and plays a crucial role in overall lipid handling. Both LXRα and LXRβ are expressed and activated by endogenous and synthetic ligands, which lead to lipid accumulation into adipocytes. This indicates an important regulatory role of LXR in several metabolic signaling pathways in the adipose tissue, such as glucose uptake and de novo fatty acid synthesis. Here, we review recent studies that provide new insights into the mechanisms by which LXRs act to influence fatty acid synthesis in liver and adipose tissue.
Original language | English (US) |
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Pages (from-to) | 59-63 |
Number of pages | 5 |
Journal | Prostaglandins Leukotrienes and Essential Fatty Acids |
Volume | 73 |
Issue number | 1 SPEC. ISS. |
DOIs | |
State | Published - Jul 2005 |
ASJC Scopus subject areas
- Clinical Biochemistry
- Cell Biology