β2-subunit alternative splicing stabilizes Cav2.3 Ca²⁺ channel activity during continuous midbrain dopamine neuron-like activity.

Abstract

In dopaminergic (DA) <i>Substantia nigra</i> (SN) neurons Cav2.3 R-type Ca²⁺-currents contribute to somatodendritic Ca²⁺-oscillations. This activity may contribute to the selective degeneration of these neurons in Parkinson's disease (PD) since Cav2.3-knockout is neuroprotective in a PD mouse model. Here, we show that in tsA-201-cells the membrane-anchored β2-splice variants β2a and β2e are required to stabilize Cav2.3 gating properties allowing sustained Cav2.3 availability during simulated pacemaking and enhanced Ca²⁺-currents during bursts. We confirmed the expression of β2a- and β2e-subunit transcripts in the mouse SN and in identified SN DA neurons. Patch-clamp recordings of mouse DA midbrain neurons in culture and SN DA neurons in brain slices revealed SNX-482-sensitive R-type Ca²⁺-currents with voltage-dependent gating properties that suggest modulation by β2a- and/or β2e-subunits. Thus, β-subunit alternative splicing may prevent a fraction of Cav2.3 channels from inactivation in continuously active, highly vulnerable SN DA neurons, thereby also supporting Ca²⁺ signals contributing to the (patho)physiological role of Cav2.3 channels in PD.