Literature DB >> 17339022

Sweet dreams for LXR.

Mitchell A Lazar1, Timothy M Willson.   

Abstract

Nuclear receptors (NRs) are transcription factors whose activities are modulated by the binding of small lipophilic ligands. The liver X receptors (LXRs) are an important pair of mammalian NRs that regulate lipid metabolism upon binding to cholesterol metabolites called oxysterols. A recent report that LXR activity is also regulated by binding to glucose (Mitro et al., 2007) expands the potential role of LXR in metabolic sensing and gene regulation. However, the hydrophilic nature of glucose and its low affinity for LXR present a challenge to central dogma about the nature of the NR-ligand interaction.

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Year:  2007        PMID: 17339022     DOI: 10.1016/j.cmet.2007.02.001

Source DB:  PubMed          Journal:  Cell Metab        ISSN: 1550-4131            Impact factor:   27.287


  11 in total

1.  Liver X receptor regulates hepatic nuclear O-GlcNAc signaling and carbohydrate responsive element-binding protein activity.

Authors:  Christian Bindesbøll; Qiong Fan; Rikke C Nørgaard; Laura MacPherson; Hai-Bin Ruan; Jing Wu; Thomas Å Pedersen; Knut R Steffensen; Xiaoyong Yang; Jason Matthews; Susanne Mandrup; Hilde I Nebb; Line M Grønning-Wang
Journal:  J Lipid Res       Date:  2015-02-27       Impact factor: 5.922

Review 2.  Insulin signaling in fatty acid and fat synthesis: a transcriptional perspective.

Authors:  Roger H F Wong; Hei Sook Sul
Journal:  Curr Opin Pharmacol       Date:  2010-12       Impact factor: 5.547

Review 3.  Thyroid hormone crosstalk with nuclear receptor signaling in metabolic regulation.

Authors:  Yan-Yun Liu; Gregory A Brent
Journal:  Trends Endocrinol Metab       Date:  2009-12-16       Impact factor: 12.015

4.  Nuclear receptor liver X receptor is O-GlcNAc-modified in response to glucose.

Authors:  Elin Holter Anthonisen; Lise Berven; Sverre Holm; Maria Nygård; Hilde I Nebb; Line M Grønning-Wang
Journal:  J Biol Chem       Date:  2009-11-20       Impact factor: 5.157

5.  ChREBP, but not LXRs, is required for the induction of glucose-regulated genes in mouse liver.

Authors:  Pierre-Damien Denechaud; Pascale Bossard; Jean-Marc A Lobaccaro; Lesley Millatt; Bart Staels; Jean Girard; Catherine Postic
Journal:  J Clin Invest       Date:  2008-03       Impact factor: 14.808

6.  Hepatic glucose sensing: does flux matter?

Authors:  Masakazu Shiota; Mark A Magnuson
Journal:  J Clin Invest       Date:  2008-03       Impact factor: 14.808

Review 7.  Contribution of de novo fatty acid synthesis to hepatic steatosis and insulin resistance: lessons from genetically engineered mice.

Authors:  Catherine Postic; Jean Girard
Journal:  J Clin Invest       Date:  2008-03       Impact factor: 14.808

8.  Aberrant activation of liver X receptors impairs pancreatic beta cell function through upregulation of sterol regulatory element-binding protein 1c in mouse islets and rodent cell lines.

Authors:  Z X Meng; Y Yin; J H Lv; M Sha; Y Lin; L Gao; Y X Zhu; Y J Sun; X Han
Journal:  Diabetologia       Date:  2012-03-14       Impact factor: 10.122

9.  Susceptibility of pancreatic beta cells to fatty acids is regulated by LXR/PPARalpha-dependent stearoyl-coenzyme A desaturase.

Authors:  Karine H Hellemans; Jean-Claude Hannaert; Bart Denys; Knut R Steffensen; Cindy Raemdonck; Geert A Martens; Paul P Van Veldhoven; Jan-Ake Gustafsson; Daniel Pipeleers
Journal:  PLoS One       Date:  2009-09-29       Impact factor: 3.240

10.  The nuclear receptor cofactor, receptor-interacting protein 140, is required for the regulation of hepatic lipid and glucose metabolism by liver X receptor.

Authors:  Birger Herzog; Magnus Hallberg; Asha Seth; Angela Woods; Roger White; Malcolm G Parker
Journal:  Mol Endocrinol       Date:  2007-08-07
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