Multiplex imaging relates quantal glutamate release to presynaptic Ca<sup>2+</sup> homeostasis at multiple synapses in situ.

Jensen, Thomas P; Zheng, Kaiyu; Cole, Nicholas; Marvin, Jonathan S; Looger, Loren L; Rusakov, Dmitri A · Nat Commun · 2019

basic_science · Level V

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Abstract

Information processing by brain circuits depends on Ca<sup>2+</sup>-dependent, stochastic release of the excitatory neurotransmitter glutamate. Whilst optical glutamate sensors have enabled detection of synaptic discharges, understanding presynaptic machinery requires simultaneous readout of glutamate release and nanomolar presynaptic Ca<sup>2+</sup> in situ. Here, we find that the fluorescence lifetime of the red-shifted Ca<sup>2+</sup> indicator Cal-590 is Ca<sup>2+</sup>-sensitive in the nanomolar range, and employ it in combination with green glutamate sensors to relate quantal neurotransmission to presynaptic Ca<sup>2+</sup> kinetics. Multiplexed imaging of individual and multiple synapses in identified axonal circuits reveals that glutamate release efficacy, but not its short-term plasticity, varies with time-dependent fluctuations in presynaptic resting Ca<sup>2+</sup> or spike-evoked Ca<sup>2+</sup> entry. Within individual presynaptic boutons, we find no nanoscopic co-localisation of evoked presynaptic Ca<sup>2+</sup> entry with the prevalent glutamate release site, suggesting loose coupling between the two. The approach enables a better understanding of release machinery at central synapses.

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