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Updated: Jun 6, 2026
Ex Vivo Imaging of Cell-specific Calcium Signaling at the Tripartite Synapse of the Mouse Diaphragm
Published on: October 4, 2018
Multimodal optical imaging combining voltage-sensitive dye ElectroFluor630 with genetically encoded calcium,
Katarina D Milicevic1,2, Amal M Abdulkadir1, Kaio S Tom1
1UConn Health, School of Medicine, Department of Neuroscience, Farmington, Connecticut, United States.
Significance:
Combining genetically encoded neuronal activity indicators (GENIs), restricted to only one neuron type, with a voltage-sensitive dye (VSD) that reports pan-neuronal activity, could be beneficial for understanding neural circuits. Recently introduced far-red EF-630 may be compatible with green GENIs and could serve as an internal reference of neuronal activity for multiple GENIs.
Aim:
Here, we assess the EF-630 compatibility with several green-fluorescent-protein-based GENIs, including the calcium indicator GCaMP6f, the glutamate indicator iGluSnFR, and two voltage indicators ASAP2s, and ASAP5-Kv, for recording neuronal aggregate responses.
Approach:
Mouse brain slices expressing each GENI were stained with EF-630, and then extracellular stimulation and population optical imaging were sequentially performed at two wavelengths. In addition, cre-dependent ASAP5-Kv transgenic mice were generated and characterized.
Results:
Dual recordings provided population signals in both channels for all combinations. For each indicator pair, we quantified amplitudes and compared ON and OFF kinetics. ASAP2s and ASAP5-Kv displayed faster temporal dynamics and less temporal summation than VSD signals, suggesting the influence of cell-type-specific expression in observed kinetics.
Conclusions:
These kinetic differences underscore how both the choice of indicator pair and the targeted cell type influence the interpretation of neural population activity. Overall, our work provides the first systematic characterization of paired VSD-GENI measurements, establishing practical considerations and performance benchmarks for dual optical imaging of neuronal populations.
