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      Action mechanisms of Liver X Receptors.

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          Abstract

          The two Liver X Receptors, LXRα and LXRβ, are nuclear receptors belonging to the superfamily of ligand-activated transcription factors. They share more than 78% homology in amino acid sequence, a common profile of oxysterol ligands and the same heterodimerization partner, Retinoid X Receptor. LXRs play crucial roles in several metabolic pathways: lipid metabolism, in particular in preventing cellular cholesterol accumulation; glucose homeostasis; inflammation; central nervous system functions and water transport. As with all nuclear receptors, the transcriptional activity of LXR is the result of an orchestration of numerous cellular factors including ligand bioavailability, presence of corepressors and coactivators and cellular context i.e., what other pathways are activated in the cell at the time the receptor recognizes its ligand. In this mini-review we summarize the factors regulating the transcriptional activity and the mechanisms of action of these two receptors.

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          Author and article information

          Journal
          Biochem Biophys Res Commun
          Biochemical and biophysical research communications
          Elsevier BV
          1090-2104
          0006-291X
          Apr 11 2014
          : 446
          : 3
          Affiliations
          [1 ] Center for Nuclear Receptors and Cell Signaling, University of Houston, 3056 Cullen Blv, 77204 Houston, Texas, USA.
          [2 ] Center for Nuclear Receptors and Cell Signaling, University of Houston, 3056 Cullen Blv, 77204 Houston, Texas, USA; Department of Biosciences and Nutrition, Karolinska Institutet, Novum S-141 86, Sweden. Electronic address: jgustafs@central.uh.edu.
          Article
          S0006-291X(13)01978-5
          10.1016/j.bbrc.2013.11.077
          24300092
          b48c8ecf-f352-4deb-8b57-654b2bc3f568
          Copyright © 2013 Elsevier Inc. All rights reserved.
          History

          LXR,Nuclear receptor,Oxysterol
          LXR, Nuclear receptor, Oxysterol

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