Native metabotropic glutamate receptor 4 depresses synaptic transmission through an unusual Gαq transduction pathway

Abstract

In cerebellar cortex, mGlu₄ receptors located on parallel fibers play an essential role in normal motor function, but the molecular mechanisms involved are not yet completely understood. Using a strategy combining biochemical and electrophysiological approaches in the rodent cerebellum, we demonstrate that presynaptic mGlu₄ receptors control synaptic transmission through an atypical activation of Gα_q proteins. First, the Gα_q subunit, PLC and PKC signaling proteins present in cerebellar extracts are retained on affinity chromatography columns grafted with different sequences of the cytoplasmic domain of mGlu₄ receptor. The i2 loop and the C terminal domain were used as baits, two domains that are known to play a pivotal role in coupling selectivity and efficacy. Second, in situ proximity ligation assays show that native mGlu₄ receptors and Gα_q subunits are in close physical proximity in cerebellar cortical slices. Finally, electrophysiological experiments demonstrate that the molecular mechanisms underlying mGlu₄ receptor-mediated inhibition of transmitter release at cerebellar Parallel Fiber (PF) - Molecular Layer Interneuron (MLI) synapses involves the Gα_q-PLC signaling pathway. Taken together, our results provide compelling evidence that, in the rodent cerebellar cortex, mGlu₄ receptors act by coupling to the Gα_q protein and PLC effector system to reduce glutamate synaptic transmission.

Keywords: Cerebellar cortex; G protein; Molecular layer interneurons; Presynaptic metabotropic glutamate receptor 4; Signaling pathway; Synaptic transmission.