Constitutive expression of functional GABAB receptors in mIL-tsA58 cells requires both GABAB(1) and GABAB(2) genes

Studies of gamma -aminobutyric acid (GABA)B receptor function in heterologous cell systems have suggested that expression of two distinct seven transmembrane G-protein coupled receptor subunits is necessary for receptor activation and signal transduction. Some results suggest that both receptor proteins must be inserted into the plasma membrane to create heterodimers; however, it is possible that subunit monomers or homodimers are functional in cells which constitutively express GABA(B) receptors. A new pituitary intermediate lobe melanotrope cell clone (mIL tsA58) has been isolated which constitutively expresses GABA(B), D-2 and corticotrophin releasing factor receptors, Here, we report on characterization of the GABA(B) receptors. Solution hybridization-nuclease protection assays reveal the presence of GABA(B(1)), and GABAB(B(2)) transcripts. Western blots show GABA(B(1a)), and one of two GABA(B(2)) proteins. Addition of the GABA((B)) agonist baclofen to cultured mIL-tsA58 (mIL) cells inhibits high voltage activated Ca2+ channels, as measured by agonist-induced inhibition of the K+-depolarization-stimulated increase in Ca2+ influx. CGP55845, a GABAs antagonist, blocks the response to baclofen. Knockdown of either GABA(B(1)) or GABA(B(2)) subunits with selective antisense oligodeoxynucleotides reduced GABA(B) protein levels and completely abolished the GABA(B) receptor response in the mit cells. Taken together, these results indicate that functionally active GABA(B) receptors in mit cells require the constitutive expression of both GABA(B) genes. This is a physiologic validation of results from recombinant overexpression in naive cells and shows that the mil cell line is a useful model for studying GABA(B) receptor expression, regulation and function.