Central Presynapses Regulate Spontaneous Synaptic Vesicle Exocytosis Rate by Constraining Recycling Pool Density

Abstract

Synapses represent a fundamental unit of information transfer during cognition. They accomplish this via presynaptic vesicle exocytosis, which can occur either spontaneously or by an action potential leading to evoked release. It has been well established that evoked release is probabilistic in nature, but it has been less clear what mechanisms mediate spontaneous release. Understanding spontaneous release is important because it is an essential maintenance mechanism for synaptic connections. We propose a mechanistic framework and model of spontaneous release based on immobile vesicles in the reserve pool geometrically constraining mobile vesicles in the recycling pool, which provides a force leading to a spontaneous release rate. We experimentally support this framework using a combination of Scanning Electron Microscopy (SEM), high-resolution fluorescence microscopy techniques using pHluorin-VGlut1 and a single vesicle SGC5 reporter, and a computational model. We observe that the spontaneous release rate increases linearly with the number of vesicles but is constant in the absence of presynaptic actin. We then use an acute agent, Forskolin, to further constrain the volume of the recycling pool, leading to an increased spontaneous release rate. We show that our framework predicts the increasing spontaneous release rate experimentally observed. These results suggest that synapses constrain the density of the recycling pool to mediate spontaneous release rate via the entropic force.