Exp Mol Med.  2009 Jun;41(6):406-416. 10.3858/emm.2009.41.6.046.

Sterol-independent repression of low density lipoprotein receptor promoter by peroxisome proliferator activated receptor gamma coactivator-1alpha (PGC-1alpha)

Affiliations
  • 1Age-Related and Brain Diseases Research Center, Department of Nanopharmaceutical and Life Sciences, Department of Physiology, Kyung Hee University College of Medicine, Seoul 130-701, Korea. ykpak@khu.ac.kr

Abstract

Peroxisome proliferator activated receptor (PPAR) gamma coactivator-1alpha (PGC-1alpha) may be implicated in cholesterol metabolism since PGC-1alpha co-activates estrogen receptor alpha (ERalpha) transactivity and estrogen/ERalpha induces the transcription of LDL receptor (LDLR). Here, we show that overexpression of PGC-1alpha in HepG2 cells represses the gene expression of LDLR and does not affect the ERalpha-induced LDLR expression. PGC-1alpha suppressed the LDLR promoter-luciferase (pLR1563-luc) activity regardless of cholesterol or functional sterol-regulatory element-1. Serial deletions of the LDLR promoter revealed that the inhibition by PGC-1alpha required the LDLR promoter regions between -650 bp and -974 bp. Phosphorylation of PGC-1alpha may not affect the suppression of LDLR expression because treatment of SB202190, a p38 MAP kinase inhibitor, did not reverse the LDLR down-regulation by PGC-1alpha. This may be the first report showing the repressive function of PGC-1alpha on gene expression. PGC-1alpha might be a novel modulator of LDLR gene expression in a sterol-independent manner, and implicated in atherogenesis.

Keyword

cholesterol; liver; peroxisome-proliferator-activated receptor-gamma coactivator-1; PPARgamma; promoter regions, genetic

MeSH Terms

Base Sequence
Cell Line, Tumor
Cholesterol/metabolism
Estrogen Receptor alpha/metabolism
Gene Expression Regulation
Heat-Shock Proteins/*genetics/*metabolism
Humans
Molecular Sequence Data
Promoter Regions, Genetic
RNA, Messenger/genetics
Receptors, LDL/*genetics/*metabolism
Sterol Regulatory Element Binding Protein 2/metabolism
Transcription Factors/*genetics/*metabolism
p38 Mitogen-Activated Protein Kinases/antagonists & inhibitors
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