Characterisation of human melatonin mt(1) and MT2 receptors by CRE-luciferase reporter assay

S Conway, S J Canning, H E Howell, E S Mowat, Perry Barrett, Janice Drew, P Delagrange, D Lesieur, Peter John Morgan

Research output: Contribution to journalArticle

57 Citations (Scopus)

Abstract

A cyclic AMP response element (CRE)-luciferase reporter gene assay was used to characterise the functional responses of human melatonin mt(1) and human melatonin MT2 receptors, stably expressed in the human embryonic kidney cell line HEK293, to a series of six naphthalenic analogues of melatonin. By comparison to the observed melatonin-mediated inhibition of stimulated luciferase levels the naphthalenic series was identified as comprising agonists, partial agonists and one antagonist of melatonin mt(1) and melatonin MT2 receptor function. Three of the agonist/partial agonist members of this series were also identified as displaying a functional selectivity for the melatonin MT2 receptor. Competitive displacement of 2-[I-125]iodomelatonin binding to the ovine pars tuberalis melatonin ML1 receptor demonstrated a close correlation to the observed functional luciferase responses of the human melatonin mt(1) receptor. We conclude that the CRE-luciferase reporter gene assay provides an effective functional screening method for the pharmacological characterisation of human melatonin receptor subtypes. (C) 2000 Elsevier Science B.V. All rights reserved.

Original languageEnglish
Pages (from-to)15-24
Number of pages10
JournalEuropean Journal of Pharmacology
Volume390
Issue number1-2
DOIs
Publication statusPublished - 25 Feb 2000

Keywords

  • melatonin receptor
  • cAMP response element
  • luciferase
  • reporter gene assay
  • HEK293 cell
  • ovine pars tuberalis
  • naphthalenic ligands
  • high-affinity
  • cloning
  • expression
  • inhibition
  • MEL(1A)
  • gene
  • pharmacology
  • localization

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