Brown adipose tissue responds to cold and adrenergic stimulation by induction of FGF21

Mol Med. 2011;17(7-8):736-40. doi: 10.2119/molmed.2011.00075. Epub 2011 Feb 25.

Abstract

Fibroblast growth factor-21 (FGF21) is a pleiotropic protein involved in glucose, lipid metabolism and energy homeostasis, with main tissues of expression being the liver and adipose tissue. Brown adipose tissue (BAT) is responsible for cold-induced thermogenesis in rodents. The role of FGF21 in BAT biology has not been investigated. In the present study, wild-type C57BL/6J mice as well as a brown adipocyte cell line were used to explore the potential role of cold exposure and β3-adrenergic stimulation in the expression of FGF21 in BAT. Our results demonstrate that short-term exposure to cold, as well as β3-adrenergic stimulation, causes a significant induction of FGF21 mRNA levels in BAT, without a concomitant increase in FGF21 plasma levels. This finding opens new routes for the potential use of pharmaceuticals that could induce FGF21 and, hence, activate BAT thermogenesis.

MeSH terms

  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Adipose Tissue, Brown / cytology
  • Adipose Tissue, Brown / drug effects*
  • Adipose Tissue, Brown / metabolism
  • Adrenergic beta-Agonists / pharmacology
  • Animals
  • Cell Line, Transformed
  • Cold Temperature*
  • Dioxoles / pharmacology*
  • Fibroblast Growth Factors / blood
  • Fibroblast Growth Factors / genetics*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Oxazoles / pharmacology
  • PPAR alpha / antagonists & inhibitors
  • PPAR alpha / genetics
  • PPAR alpha / metabolism
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Adrenergic, beta-3 / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Thermogenesis / drug effects
  • Thermogenesis / genetics
  • Trans-Activators / genetics
  • Transcription Factors
  • Transcriptional Activation / drug effects
  • Tyrosine / analogs & derivatives
  • Tyrosine / pharmacology

Substances

  • Adrenergic beta-Agonists
  • Dioxoles
  • GW 6471
  • Oxazoles
  • PPAR alpha
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Ppargc1a protein, mouse
  • RNA, Messenger
  • Receptors, Adrenergic, beta-3
  • Trans-Activators
  • Transcription Factors
  • fibroblast growth factor 21
  • disodium (R,R)-5-(2-((2-(3-chlorophenyl)-2-hydroxyethyl)-amino)propyl)-1,3-benzodioxole-2,3-dicarboxylate
  • Tyrosine
  • Fibroblast Growth Factors