Multiplex imaging relates quantal glutamate release to presynaptic Ca<sup>2+</sup> homeostasis at multiple synapses in situ.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30926781.
- Also identified by DOI 10.1038/s41467-019-09216-8 and PMC identifier 6441074.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
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.
Medical subject headings
- Calcium
- Glutamic Acid
- Homeostasis
- Imaging, Three-Dimensional
- Presynaptic Terminals