Identification of human low-density lipoprotein receptor as a novel target gene regulated by liver X receptor alpha

被引:42
作者
Ishimoto, Kenji
Tachibana, Keisuke
Sumitomo, Mikako
Omote, Shiho
Hanano, Ikuko
Yamasaki, Daisuke
Watanabe, Yuichiro
Tanaka, Toshiya
Hamakubo, Takao
Sakai, Juro
Kodama, Tatsuhiko
Doi, Takefumi
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Suita, Osaka 5650871, Japan
[2] Univ Tokyo, Lab Syst Biol & Med, Adv Sci & Technol Res Ctr, Tokyo, Japan
[3] Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, Pharmacol Grp, Tokyo, Japan
[4] Osaka Univ, Grad Sch Med, Osaka, Japan
关键词
liver X receptor; low-density lipoprotein receptor; cholesterol; LXR response element; nuclear receptor; SREBP;
D O I
10.1016/j.febslet.2006.08.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Liver X receptor alpha (LXR alpha) is a member of the nuclear receptor superfamily that is activated by oxysterols, and plays a pivotal role in regulating the metabolism, transport and uptake of cholesterol. Here, we demonstrate that LXR alpha also regulates the low-density lipoprotein receptor (LDLR) gene, which mediates the endocytic uptake of LDL cholesterol in the liver. An LXR agonist induced the expression of LDLR in cultured hepatoblastoma cells. Moreover, the LDLR promoter contained an LXR response element that was recognized by LXR alpha/RXR alpha (retinoid X receptor alpha) heterodimers in hepatoblastoma cells. These results suggest a novel pathway whereby LXR alpha might modulate cholesterol metabolism. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:4929 / 4933
页数:5
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