Hepatocyte nuclear factor-4α plays pivotal roles in the regulation of mouse carboxylesterase 2 gene transcription in mouse liver

被引:35
|
作者
Furihata, T
Hosokawa, M [1 ]
Masuda, M
Satoh, T
Chiba, K
机构
[1] Chiba Inst Sci, Fac Pharmaceut Sci, Lab Drug Metab & Biopharmaceut, Choshi, Chiba 2880025, Japan
[2] Chiba Univ, Grad Sch Pharmaceut Sci, Lab Pharmacol & Toxicol, Chiba 2608675, Japan
关键词
carboxylesterase; hepatocyte nuclear factor-4 alpha; small heterodimer partner; chenodeoxycholic acid; TLR2; cells;
D O I
10.1016/j.abb.2006.01.015
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
The Mouse carboxylesterase 2 isozyme, mCES2, is thought to play important roles in lipid metabolism and is expressed in the liver, kidney, and small intestine at high levels. In this Study, we examined the molecular mechanisms controlling this tissue-specific-expression of mCES2, and demonstrated that hepatocyte nuclear factor-4 alpha. (HNF-4 alpha) could enhance transcription of the mCES2 gene in vitro and in vivo. It Was found that effects of HNF-4 alpha on the level of mCES2 promoter activity were repressed by small heterodimer partner (SHP) and chenodeoxycholic acid (CDCA) in luciferase assays. Accordingly, mCES2 gene transcription was repressed by CDCA treatment in mouse immortalized hepatocytes. Our results suggested that this repression resulted from the combined effects of both inhibition of HNF4 alpha transactivation ability by SHP and reduction of HNF-4 alpha expression level. These findings show that HNF-4 alpha plays an important role in the regulation of mCES2 gene transcription. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:107 / 117
页数:11
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