Dopamine receptor type 2 (D2R) and ghrelin receptor (GHSR) co-expression alters Ca V 2.2 modulation by G protein signaling cascades.

MUSTAFÁ, EMILIO ROMÁN; RAINGO, JESICA; CORDISCO GONZALEZ, SANTIAGO; PERELLO, MARIO; RODRIGUEZ, SILVIA S.

ACS Chemical Neuroscience

ACS publications

Lugar: Washington; Año: 2019 vol. 11 p. 3 - 13

1948-7193

Voltage-gated calcium channels type 2.2 (CaV2.2) are activated by action potentials at presynaptic terminals, and their calcium current induces neurotransmitter release. In this context, regulating CaV2.2 is critical, and one of the most important mechanisms for doing so is through is G protein-coupled receptor (GPCR) activity. Two such GPCRs are the ghrelin (GHSR) and the dopamine type 2 (D2R) receptors. We previously demonstrated that constitutive GHSR activity reduces CaV2.2 forward trafficking and that ghrelin-induced GHSR activity inhibits CaV2.2 currents. On the other hand, dopamine-induced D2R activity also inhibits CaV2.2 currents. It has been recently shown that D2R and GHSR form heteromers in hypothalamic neurons. This interaction profoundly changes the signaling cascades activated by dopamine and is necessary for dopamine-dependent anorexia. Here we explored how D2R-GHSR co-expression in HEK293T cells modulates the effect that each GPCR has on CaV2.2. We found that D2R-GHSR co-expression reduces the inhibition of CaV2.2 currents by agonist-induced D2R activation and added a new source of basal CaV2.2 current inhibition to the one produced by GHSR solely expression. We investigated the signaling cascades implicated and found that constitutive GHSR activity, Gq protein and Gβγ subunit play a critical role in these altered effects. Moreover, we found that the effect of D2R agonist on native calcium currents in hypothalamic neurons is reduced when both D2R and GHSR are over-expressed. In summary, our results allow us to propose a novel mechanism for controlling CaV2.2 currents involving the co-expression of two physiologically relevant GPCRs