Dopamine D2 and Adenosine A2A Receptors Regulate NMDA-Mediated Excitation in Accumbens Neurons Through A2A|[ndash]|D2 Receptor Heteromerization

摘要

Bursting activity of striatal medium spiny neurons results from membrane potential oscillations between a down- and an upstate that could be regulated by G-protein-coupled receptors. Among these, dopamine D2 and adenosine A2A receptors are highly enriched in striatal neurons and exhibit strong interactions whose physiological significance and molecular mechanisms remain partially unclear. More particularly, respective involvements of common intracellular signaling cascades and A2A–D2 receptor heteromerization remain unknown. Here we show, by performing perforated-patch-clamp recordings on brain slices and loading competitive peptides, that D2 and A2A receptors regulate the induction by N-methyl-D-aspartate of a depolarized membrane potential plateau through mechanisms relying upon specific protein–protein interactions. Indeed, D2 receptor activation abolished transitions between a hyperpolarized resting potential and a depolarized plateau potential by regulating the CaV1.3a calcium channel activity through interactions with scaffold proteins Shank1/3. Noticeably, A2A receptor activation had no effect per se but fully reversed the effects of D2 receptor activation through a mechanism in which A2A–D2 receptors heteromerization is strictly mandatory, demonstrating therefore a first direct physiological relevance of these heteromers. Our results show that membrane potential transitions and firing patterns in striatal neurons are tightly controlled by D2 and A2A receptors through specific protein–protein interactions including A2A–D2 receptors heteromerization.