ß2-Adrenergic Receptors Chaperone Trapped Bitter Taste Receptor 14 to the Cell Surface as a Heterodimer and Exert Unidirectional Desensitization of Taste Receptor Function.

ABSTRACT

Bitter taste receptors (TAS2Rs) are G-protein-coupled receptors now recognized to be expressed on extraoral cells, including airway smooth muscle (ASM) where they evoke relaxation. TAS2Rs are difficult to express in heterologous systems, with most receptors being trapped intracellularly. We find, however, that co-expression of ß2-adrenergic receptors (ß2AR) in HEK-293T routes TAS2R14 to the cell surface by forming receptor heterodimers. Cell surface TAS2R14 expression was increased by ∼5-fold when ß2AR was co-expressed. Heterodimer formation was shown by co-immunoprecipitation with tagged receptors, biomolecular fluorescence complementation, and merged confocal images. The dynamic nature of this interaction was shown by a gene-dose relationship between transfected ß2AR and TAS2R14 expression, enhanced (up to 3-fold) TAS2R14 agonist stimulation of [Ca(2+)]i with ß2AR co-transfection, ∼53% decrease in [Ca(2+)]i signaling with shRNA knockdown of ß2AR in H292 cells, and ∼60% loss of [Ca(2+)]i responsiveness in ßAR knock-out mouse ASM. Once expressed on the surface, we detected unidirectional, conformation-dependent, interaction within the heterodimer, with ß2AR activation rapidly uncoupling TAS2R14 function (∼65% desensitization). Cross-talk was independent of ß2AR internalization and cAMP/PKA, and not accompanied by TAS2R14 internalization. With prolonged ß-agonist exposure, TAS2R14 internalized, consistent with slow recycling of naked TAS2R14 in the absence of the heterodimeric milieu. In studies of ASM mechanics, rapid cross-talk was confirmed at the physiologic level, where relaxation from TAS2R14 agonist was decreased by ∼50% with ß-agonist co-treatment. Thus the ß2AR acts as a double-edged sword increasing TAS2R14 cell surface expression, but when activated by ß-agonist, partially offsetting the expression phenotype by direct receptorreceptor desensitization of TAS2R14 function.