The rat D4 dopamine receptor couples to cone transducin (Gα(t2)) to inhibit forskolin-stimulated cAMP accumulation

Ikuyo Yamaguchi, Steven K. Harmon, Richard D. Todd, Karen L. O'Malley

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

Based on its expression pattern and pharmacology, the D4 dopamine receptor may play a role in schizophrenia. Thus it is of interest to know what signaling pathways are utilized by this receptor. Previously, we showed that activation of D4 receptors in a mouse mesencephalic neuronal cell line (MN9D) inhibited forskolin-stimulated cAMP accumulation in a pertussis toxin- sensitive (Ptx-sensitive) fashion. Of the known Ptx-sensitive G-protein α subunits, MN9D-expressed Gα(t2), Gα(oA), and Gα(oB); however, none of these coupled to the D4 receptor. Using a low stringency polymerase chain reaction cloning method, we found an additional Ptx-sensitive G-protein cone transducin (Gα(t2)) expressed in the MN9D cells. We also found that Gα(t2) mRNA is highly expressed in rat mesencephalic tissue. To test the hypothesis that the D4 receptor couples to Gα(t2), we cotransfected MN9D cells with the D4 receptor and a mutagenized Ptx-resistant Gα(t2) subunit (mGα(t2)). Application of the dopaminergic agonist quinpirole to cotransfected cells inhibited forskolin-stimulated cAMP accumulation in the presence or absence of Ptx. To our knowledge, this is the first report demonstrating that the D4 dopamine receptor functionally couples to a specific G-protein and that a non-opsin-like receptor can couple with a transducin subunit.

Original languageEnglish (US)
Pages (from-to)16599-16602
Number of pages4
JournalJournal of Biological Chemistry
Volume272
Issue number26
DOIs
StatePublished - Jun 27 1997

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Fingerprint Dive into the research topics of 'The rat D<sub>4</sub> dopamine receptor couples to cone transducin (Gα(t2)) to inhibit forskolin-stimulated cAMP accumulation'. Together they form a unique fingerprint.

Cite this