Quantitation of single action potential-evoked Ca2+ signals in CA1 pyramidal neuron presynaptic terminals

Abstract

Presynaptic Ca2+ evokes exocytosis, endocytosis, and short-term synaptic plasticity. However, Ca2+ flux and interactions at presynaptic molecular targets are difficult to determine, because imaging has limited resolution. We measured single varicosity presynaptic Ca2+ using Ca2+ dyes as buffers, and constructed models of Ca2+ dispersal. Action potentials evoked Ca2+ transients (peak amplitude, 789{+/-}39 nM, within 2 ms of stimulation; decay times, 119{+/-}10 ms) with little variation when measured with low-affinity dye. Endogenous Ca2+ buffering capacities, action potential-evoked free [Ca2+]{inverted exclamation} and total amounts entering terminals were determined using high-affinity Ca2+ dyes to buffer Ca2+ transients. These data constrained Monte Carlo (MCell) simulations of Ca2+ entry, buffering, and removal. Data were well-fit with simulations of experimentally-determined Ca2+ fluxes, buffered by simulated Calbindin28K. Simulations were consistent with clustered Ca2+ entry followed within 2 ms by diffusion throughout the varicosity. Repetitive stimulation caused free varicosity Ca2+ to sum. However, simulated in nanometer domains, its removal by pumps and buffering was negligible, while diffusion rates were high. Thus, Ca2+ within tens of nanometers of entry, did not accumulate during sequential stimuli. A model of synaptotagmin1-Ca2+ binding indicates that even with 10 M free varicosity Ca2+, synaptogmin1 must be within tens of nanometers of channels to ensure occupation of all its Ca2+ binding sites. Repetitive stimulation, which evokes short-term synaptic enhancement, does not modify probabilities of Ca2+ fully occupying synaptotagmin1s C2 domains, suggesting that enhancement is not mediated by Ca2+-synaptotagmin1. We conclude that at spatio-temporal scale of fusion machines, Ca2+ necessary for their activation is diffusion dominated.