Interleukin-1beta suppresses retinoid transactivation of two hepatic transporter genes involved in bile formation

J Biol Chem. 2000 Mar 24;275(12):8835-43. doi: 10.1074/jbc.275.12.8835.

Abstract

Cytokines have been implicated in the pathogenesis of inflammatory cholestasis. This is due to transcriptional down-regulation of hepatic transporters including the Na(+)/bile acid cotransporter, ntcp, and the multispecific organic anion exporter, mrp2. We have recently shown that ntcp suppression by lipopolysaccharide in vivo is caused by down-regulation of transactivators including the previously uncharacterized Footprint B-binding protein. Both the ntcp FpB element and the mrp2 promoter contain potential retinoid-response elements. We hypothesized that retinoic acid receptor (RAR) and retinoid X receptor (RXR) heterodimers would activate these two genes and that cytokines that reduce bile flow might do so by suppressing nuclear levels of these transactivators. Retinoid transactivation and interleukin-1beta down-regulation of the ntcp and mrp2 promoters were mapped to RXRalpha:RARalpha-response elements. Gel mobility shift assays demonstrated specific binding of RXRalpha:RARalpha heterodimers to the ntcp and mrp2 retinoid-response elements. The RXRalpha:RARalpha complex was down-regulated by IL-1beta in HepG2 cells. An unexpected finding was that an adjacent CAAT-enhancer-binding protein element was required for maximal transactivation of the ntcp promoter by RXRalpha:RARalpha. Taken together, these studies demonstrate regulation of two hepatobiliary transporter genes by RXRalpha:RARalpha and describe a mechanism which likely contributes to their down-regulation during inflammation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Albumins / genetics
  • Animals
  • Anion Transport Proteins
  • Bile / metabolism*
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics*
  • Cholestasis / etiology
  • Cytokines / pharmacology
  • DNA-Binding Proteins / metabolism
  • Dimerization
  • Humans
  • Interleukin-1 / pharmacology*
  • Interleukin-6 / genetics
  • Liver / metabolism*
  • Membrane Transport Proteins*
  • Mutation
  • Nuclear Proteins / metabolism
  • Organic Anion Transporters, Sodium-Dependent
  • Promoter Regions, Genetic
  • Protein Binding
  • Protein Isoforms / metabolism
  • Rats
  • Receptors, Retinoic Acid / metabolism
  • Recombinant Fusion Proteins / biosynthesis
  • Response Elements
  • Retinoid X Receptors
  • Retinoids / pharmacology*
  • Symporters
  • Transcription Factors / metabolism
  • Transcriptional Activation*

Substances

  • Albumins
  • Anion Transport Proteins
  • Carrier Proteins
  • Cytokines
  • DNA-Binding Proteins
  • Interleukin-1
  • Interleukin-6
  • Membrane Transport Proteins
  • Nuclear Proteins
  • Organic Anion Transporters, Sodium-Dependent
  • Protein Isoforms
  • Receptors, Retinoic Acid
  • Recombinant Fusion Proteins
  • Retinoid X Receptors
  • Retinoids
  • Symporters
  • Transcription Factors
  • sodium-bile acid cotransporter