LXRs AND FXR: The Yin and Yang of cholesterol and fat metabolism

被引:481
作者
Kalaany, NY [1 ]
Mangelsdorf, DJ
机构
[1] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] Univ Texas, SW Med Ctr, Howard Hughes Med Inst, Dallas, TX 75390 USA
关键词
nuclear receptors; liver X receptors; farnesoid X receptor; bile acids; lipid metabolism;
D O I
10.1146/annurev.physiol.68.033104.152158
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Liver X receptors (LXRs) and farnesoid X receptor (FXR) are nuclear receptors that function as intracellular sensors for sterols and bile acids, respectively. In response to their ligands, these receptors induce transcriptional responses that maintain a balanced, finely tuned regulation of cholesterol and bile acid metabolism. LXRs also permit the efficient storage of carbohydrate- and fat-derived energy, whereas FXR activation results in an overall decrease in triglyceride levels and modulation of glucose metabolism. The elegant, dual interplay between these two receptor systems Suggests that they coevolved to Constitute a highly sensitive and efficient system for the maintenance of total body fat and cholesterol homeostasis. Emerging evidence suggests that the tissue-specific action of these receptors is also Crucial for the proper function of the cardiovascular, immune, reproductive, endocrine pancreas, renal, and central nervous systems. Together, LXRs and FXR represent potential therapeutic targets for the treatment and prevention of numerous metabolic and lipid-related diseases.
引用
收藏
页码:159 / 191
页数:33
相关论文
共 196 条
[1]  
ALBERS JJ, 1982, GASTROENTEROLOGY, V82, P638
[2]   Human bile salt export pump promoter is transactivated by the farnesoid X receptor/bile acid receptor [J].
Ananthanarayanan, M ;
Balasubramanian, N ;
Makishima, M ;
Mangelsdorf, DJ ;
Suchy, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (31) :28857-28865
[3]   Inactivation of liver X receptor β leads to adult-onset motor neuron degeneration in male mice [J].
Andersson, S ;
Gustafsson, N ;
Warner, M ;
Gustafsson, JÅ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (10) :3857-3862
[4]  
ANGELIN B, 1978, J LIPID RES, V19, P1017
[5]   Activation of the nuclear receptor FXR induces fibrinogen expression: a new role for bile acid signaling [J].
Anisfeld, AM ;
Kast-Woelbern, HR ;
Lee, H ;
Zhang, YQ ;
Lee, FY ;
Edwards, PA .
JOURNAL OF LIPID RESEARCH, 2005, 46 (03) :458-468
[6]   Syndecan-1 expression is regulated in an isoform-specific manner by the farnesoid-X receptor [J].
Anisfeld, AM ;
Kast-Woelbern, HR ;
Meyer, ME ;
Jones, SA ;
Zhang, YQ ;
Williams, KJ ;
Willson, T ;
Edwards, PA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (22) :20420-20428
[7]   A role for the apoptosis inhibitory factor AIM/Spα/Api6 in atherosclerosis development [J].
Arai, S ;
Shelton, JM ;
Chen, MY ;
Bradley, MN ;
Castrillo, A ;
Bookout, AL ;
Mak, PA ;
Edwards, PA ;
Mangelsdorf, DJ ;
Tontonoz, P ;
Miyazaki, T .
CELL METABOLISM, 2005, 1 (03) :201-213
[8]   Neither intestinal sequestration of bile acids nor common bile duct ligation modulate the expression and function of the rat ileal bile acid transporter [J].
Arrese, M ;
Trauner, M ;
Sacchiero, RJ ;
Crossman, MW ;
Shneider, BL .
HEPATOLOGY, 1998, 28 (04) :1081-1087
[9]  
Auwerx J, 1999, CELL, V97, P161
[10]   FXR induces the UGT2B4 enzyme in hepatocytes: A potential mechanism of negative feedback control of FXR activity [J].
Barbier, O ;
Torra, IP ;
Sirvent, A ;
Claudel, T ;
Blanquart, C ;
Duran-Sandoval, D ;
Kuipers, F ;
Kosykh, V ;
Fruchart, JC ;
Staels, B .
GASTROENTEROLOGY, 2003, 124 (07) :1926-1940