G-protein coupled receptors (GPCRs) are one of the largest membrane protein families in eukaryotes and mediates various important function of the cells. Recently, there is increasing evidence that several GPCRs may form complexes, and complexed GPCRs may mutually regulate their function. Previous reports including ours unveiled the interaction between two GPCRs expressed in neurons, type 1 metabotropic glutamate receptor (mGluR1) and gamma-aminobutyric acid B receptor (GABABR). mGluR1 is expressed particularly in cerebellum and known to play crucial roles in synaptic plasticity and motor learning. GABABR is widely expressed in central nervous system and regulates neuronal excitability. Our previous study suggested that GABABR modulates mGluR1-mediated synaptic plasticity in cerebellar Purkinje cell. In this study, we showed the mechanism underlying modulation between mGluR1 and GABABR. Biochemical analysis and molecular imaging assay showed that mGluR1 form complexes with GABABR at the cell membrane. Moreover, an assay monitored intracellular signaling transduction revealed functional interaction between these GPCRs. Our findings provide a novel insight into the regulatory mechanism of synaptic plasticity and motor learning, and indicate that complex formation and functional interaction between distinct GPCRs might have significant roles under physiological and pathophysiological conditions.

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