In vivo imaging of farnesoid X receptor activity reveals the ileum as the primary bile acid signaling tissue

Mol Endocrinol. 2007 Jun;21(6):1312-23. doi: 10.1210/me.2007-0113. Epub 2007 Apr 10.


We generated and characterized a firefly luciferase reporter mouse for the nuclear receptor farnesoid X receptor (FXR). This FXR reporter mouse has basal luciferase expression in the terminal ileum, an organ with well-characterized FXRalpha signaling. In vivo luciferase activity reflected the diurnal activity pattern of the mouse, and is regulated by both natural (bile acids, chenodeoxycholic acid) and synthetic (GW4064) FXRalpha ligands. Moreover, in vivo and in vitro analysis showed luciferase activity after GW4064 administration in the liver, kidney, and adrenal gland, indicating that FXRalpha signaling is functional in these tissues. Hepatic luciferase activity was robustly induced in cholestatic mice, showing that FXRalpha signaling pathways are activated in this disease. In conclusion, we have developed an FXR reporter mouse that is useful to monitor FXRalpha signaling in vivo in health and disease. The use of this animal could facilitate the development of new therapeutic compounds that target FXRalpha in a tissue-specific manner.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Glands / chemistry
  • Adrenal Glands / metabolism
  • Animals
  • Bile Acids and Salts / metabolism*
  • Bile Acids and Salts / pharmacology
  • Chenodeoxycholic Acid / pharmacology
  • DNA-Binding Proteins / agonists
  • DNA-Binding Proteins / metabolism*
  • Genes, Reporter / drug effects
  • Ileum / chemistry
  • Ileum / metabolism*
  • Isoxazoles / pharmacology
  • Kidney / chemistry
  • Kidney / metabolism
  • Ligands
  • Liver / chemistry
  • Liver / metabolism
  • Luciferases / analysis
  • Luciferases / genetics
  • Mice
  • Mice, Transgenic
  • Models, Animal
  • Receptors, Cytoplasmic and Nuclear / agonists
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Signal Transduction
  • Transcription Factors / agonists
  • Transcription Factors / metabolism*


  • Bile Acids and Salts
  • DNA-Binding Proteins
  • Isoxazoles
  • Ligands
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • farnesoid X-activated receptor
  • Chenodeoxycholic Acid
  • Luciferases
  • GW 4064