FXR-mediated down-regulation of CYP7A1 dominates LXRα in long-term cholesterol-fed NZW rabbits

被引:34
作者
Xu, GR [1 ]
Li, H
Pan, LX
Shang, Q
Honda, A
Ananthanarayanan, M
Erickson, SK
Shneider, BL
Shefer, S
Bollineni, J
Forman, BM
Matsuzaki, Y
Suchy, FJ
Tint, GS
Salen, G
机构
[1] Vet Adm Med Ctr, Med Serv, E Orange, NJ 07018 USA
[2] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Med, Newark, NJ 07103 USA
[3] Univ Tsukuba, Sch Med, GI Div, Tsukuba, Ibaraki 3058575, Japan
[4] Mt Sinai Med Ctr, Dept Pediat, New York, NY 10029 USA
[5] Univ Calif San Francisco, Dept Med, San Francisco, CA 94121 USA
[6] Vet Adm Med Ctr, San Francisco, CA 94121 USA
[7] City Hope Natl Med Ctr, Dept Mol Med, Duarte, CA 91010 USA
关键词
dietary cholesterol; oxysterol; short-heterodimer partner; ATP binding cassette transporter A1;
D O I
10.1194/jlr.M300182-JLR200
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
We investigated how cholesterol feeding regulates cholesterol 7alpha-hydroxylase (CYP7A1) via the nuclear receptors farnesoid X receptor (FXR) and liver X receptor alpha (LXRalpha) in New Zealand white rabbits. After 1 day of 2% cholesterol feeding, when the bile acid pool size had not expanded, mRNA levels of the FXR target genes short-heterodimer partner (SUP) and sterol 12alpha-hydroxylase (CYP8B) were unchanged, indicating that FXR activation remained constant. In contrast, the mRNA levels of the LXRalpha target genes ATP binding cassette transporter A1 (ABCA1) and cholesteryl ester transfer protein (CETP) increased 5-fold and 2.3-fold, respectively, associated with significant increases in hepatic concentrations of oxysterols. Activity and mRNA levels of CYP7A1 increased 2.4 times and 2.2 times, respectively. After 10 days of cholesterol feeding, the bile acid pool size increased nearly 2-fold. SHP mRNA levels increased 4.1-fold while CYP8B declined 64%. ABCA1 mRNA rose 8-fold and CETP mRNA remained elevated. Activity and mRNA of CYP7A1 decreased 60% and 90%, respectively. Feeding cholesterol for 1 day did not enlarge the ligand pool size or change FXR activation, while LXRalpha was activated highly secondary to increased hepatic oxysterols. As a result, CYP7A1 was up-regulated. After 10 days of cholesterol feeding, the bile acid (FXR ligand) pool size increased, which activated FXR and inhibited CYP7A1 despite continued activation of LXRalpha. jlr Thus, in rabbits, when FXR and LXRalpha are activated simultaneously, the inhibitory effect of FXR overrides the stimulatory effect of LXRalpha to suppress CYP7A1 mRNA expression.-Xu, G., H. Li, L-x. Pan, Q. Shang, A. Honda, M. Ananthanarayanan, S. K Erickson, B. L. Shneider, S. Shefer, J. Bollineni, B. M. Forman, Y. Matsuzaki, E J. Suchy, G. S. Tint, and G. Salen. FXR-mediated down-regulation of CYP7A1 dominates LXRalpha in long-term cholesterol fed NZW rabbits. J. Lipid Res. 2003. 44: 1956-1962.
引用
收藏
页码:1956 / 1962
页数:7
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