Stable expression of human D3 dopamine receptors in GH4C1 pituitary cells

Abstract

Human D₃ dopamine receptor DNA was stably transfected into GH₄C₁ pituitary cells. Displacement of iodosulpiride binding in hD3 transfected cells (K_d = 0.3 nM, B _max = 89 fmol/mg protein) by dopaminergic ligands was indistinguishable from that of hD3 receptors in CHO cells. Only two clonal cell lines exhibited weak GppNHp-dependent shifts in [³H]N-0437 binding, and these were used for functional assays. Neither arachidonic acid metabolism, cAMP levels, inositol phosphate turnover, intracellular calcium, or potassium currents were consistently affected by dopamine (1–10 μM). The paucity of responses indicates that human D₃ receptors do not couple efficiently to these second messengers in GH₄C₁ cells.