Inflammation inhibits GPR81 expression in adipose tissue

Inflamm Res. 2011 Oct;60(10):991-5. doi: 10.1007/s00011-011-0361-2. Epub 2011 Jul 13.

Abstract

Objective and design: The aim of this study was to examine the expression of G protein-coupled receptor 81 (GPR81) in mouse adipose tissue in response to inflammatory stimuli. GPR81 is activated by lactate resulting in the inhibition of lipolysis.

Materials and treatment: Mice were injected with saline, lipopolysaccharide (LPS), zymosan, or turpentine, N = 5 per group. 3T3-L1 adipocytes were treated with tumor necrosis factor alpha, interleukin (IL)-l beta, IL-6, or interferon gamma.

Methods: GPR81 expression levels were measured by real-time PCR and statistical significance was determined by Student's t test.

Results: LPS resulted in a marked decrease in GPR81 mRNA level in mouse adipose tissue in C57BL/6 and OuJ mice, an effect that was not observed in HeJ mice, which have a mutation in TLR4. Zymosan and turpentine also decreased adipose tissue GPR81 expression. Cytokine treatment of 3T3-L1 adipocytes had no effect on GPR81 expression. GPR81 expression was decreased in ob/ob mice, an animal model of type 2 diabetes that is characterized by inflammation.

Conclusion: Inflammation decreases the expression of GPR81 in adipose tissue.

Publication types

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

MeSH terms

  • 3T3-L1 Cells / cytology
  • Adipocytes / metabolism
  • Adipose Tissue / metabolism*
  • Animals
  • Cytokines / metabolism
  • Female
  • Gene Expression Regulation*
  • Inflammation / metabolism*
  • Interferon-gamma / biosynthesis
  • Interleukin-1beta / biosynthesis
  • Interleukin-6 / biosynthesis
  • Lipolysis
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Receptors, G-Protein-Coupled / biosynthesis*
  • Toll-Like Receptor 4 / metabolism

Substances

  • Cytokines
  • Hcar1 protein, mouse
  • Interleukin-1beta
  • Interleukin-6
  • Receptors, G-Protein-Coupled
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • Interferon-gamma