Excitatory and Inhibitory Neurons Utilize Different Ca2+ Sensors and Sources to Regulate Spontaneous Release

Abstract

Spontaneous neurotransmitter release (mini) is an important form of Ca²⁺-dependent synaptic transmission that occurs in the absence of action potentials. A molecular understanding of this process requires an identification of the underlying Ca²⁺ sensors. Here, we address the roles of the relatively low- and high-affinity Ca²⁺ sensors, synapotagmin-1 (syt1) and Doc2α/β, respectively. We found that both syt1 and Doc2 regulate minis, but, surprisingly, their relative contributions depend on whether release was from excitatory or inhibitory neurons. Doc2α promoted glutamatergic minis, while Doc2β and syt1 both regulated GABAergic minis. We identified Ca²⁺ ligand mutations in Doc2 that either disrupted or constitutively activated the regulation of minis. Finally, Ca²⁺ entry via voltage-gated Ca²⁺ channels triggered miniature GABA release by activating syt1, but had no effect on Doc2-driven minis. This work reveals an unexpected divergence in the regulation of spontaneous excitatory and inhibitory transmission in terms of both Ca²⁺ sensors and sources.

Keywords: Doc2; calcium sensor; membrane fusion; miniature release; neurotransmission; neurotransmitter; spontaneous release; synaptic transmission; synaptotagmin I.