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Characterization of a cloned rat serotonin 5-HT1A receptor expressed in the HeLa cell line

  • Yutaka Fujiwara
  • , Hiroaki Tomita
  • , Mitsuru Hikiji
  • , Kenichi Kashihara
  • , Saburo Otsuki
  • , Tetsuo Ohnuki
  • , Yasutaro Hamagishi
  • , Toshikazu Oki
  • , Ichiro Sora
  • , William R. Roeske
  • , Henry I. Yamamura

Research output: Contribution to journalArticlepeer-review

Abstract

We have previously isolated the rat serotonin (5-HT)1A receptor gene (G21Y2) and now report the expression and characterization of this receptor. The BamHl/Xbal fragment of this gene was cloned into Rc/RSV and stably transfected into HeLa cells by the calcium phosphate method. For determination of specific 5-HT1A receptor binding, [3H]8OH-DPAT was used as the radioligand and incubated with HeLa cell membranes. The cells expressed specific and saturable binding of [3H]8OH-DPAT with a Kd value of 0.3 nM and a Bmax value of 2 pmol/mg protein. GTP (50 μM) added to the incubation mixture increased the Kd value to 3 nM indicating that the expressed receptor is coupled to a G protein. The specific binding was inhibited by selective 5-HT1A partial agonists, such as buspirone, ipsapirone, gepirone, tandospirone, zalospirone and SUN8399 with Ki values of 1-30nM, whereas other neurotropic drugs except for spiperone (Ki=46 nM) and nemonapride (Ki=2.3 nM) were effective only at concentrations of more than 100 μM. The potencies of these compounds to inhibit [3H]8OH-DPAT from its specific binding sites were similar to their affinities determined in rat hippocampus binding studies. These data suggest that the expressed receptor is a 5-HT1A-type similar to 5-HT1A receptors in the rat hippocampus.

Original languageEnglish (US)
Pages (from-to)949-958
Number of pages10
JournalLife Sciences
Volume52
Issue number11
DOIs
StatePublished - 1993

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology
  • General Pharmacology, Toxicology and Pharmaceutics

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