Stable expression of human melanocortin 3 receptor fused to EGFP in the HEK293 cells

Biochem Biophys Res Commun. 2003 Jun 20;306(1):208-12. doi: 10.1016/s0006-291x(03)00934-3.

Abstract

Among the melanocortins alpha-MSH is known to be involved in feeding behavior. These hormones mediate their effects through G protein-coupled receptors by stimulating adenylate cyclase. In this study, we have developed an in vitro expression model for human melanocortin 3 receptor (hMC3R) tagged at its C terminus with EGFP. The corresponding chimeric cDNA was stably expressed in HEK293 cells. The selected clones expressing the hMC3R-EGFP exhibited cell surface fluorescence and responded to NDP-MSH stimulation by producing cAMP in a dose-dependent manner (EC(50): 0.3 nM). Binding studies revealed a single class of binding sites with a K(D) of 2.24 nM. Moreover, Agouti-related protein was also demonstrated to be an antagonist of the hMC3R-EGFP. Thus, the hMC3R tagged with EGFP stably expressed in HEK293 cells, exhibiting the same characteristics than the wild-type hMC3R, is the only model of expression of this receptor allowing its direct localization inside living cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Binding Sites
  • Cell Line
  • Cyclic AMP / biosynthesis
  • DNA, Complementary / genetics
  • Gene Expression
  • Green Fluorescent Proteins
  • Humans
  • Kinetics
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Microscopy, Confocal
  • Microscopy, Fluorescence
  • Receptor, Melanocortin, Type 3
  • Receptors, Corticotropin / genetics*
  • Receptors, Corticotropin / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • alpha-MSH / analogs & derivatives*
  • alpha-MSH / pharmacology

Substances

  • DNA, Complementary
  • Luminescent Proteins
  • Receptor, Melanocortin, Type 3
  • Receptors, Corticotropin
  • Recombinant Fusion Proteins
  • Green Fluorescent Proteins
  • alpha-MSH
  • MSH, 4-Nle-7-Phe-alpha-
  • Cyclic AMP