Two-photon imaging of Zn[superscript 2+] dynamics in mossy fiber boutons of adult hippocampal slices

Mossy fiber termini in the hippocampus accumulate Zn[superscript 2+], which is released with glutamate from synaptic vesicles upon neural excitation. Understanding the spatiotemporal regulation of mobile Zn[superscript 2+] at the synaptic level is challenging owing to the difficulty of visualizing...

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Bibliographic Details
Main Authors: Khan, Mustafa, Goldsmith, Christian R., Huang, Zhen, Georgiou, John, Luyben, Thomas T., Roder, John C., Lippard, Stephen J., Okamoto, Kenichi
Other Authors: Massachusetts Institute of Technology. Department of Chemistry
Format: Article
Language:en_US
Published: National Academy of Sciences (U.S.) 2014
Online Access:http://hdl.handle.net/1721.1/91965
https://orcid.org/0000-0002-2693-4982
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Summary:Mossy fiber termini in the hippocampus accumulate Zn[superscript 2+], which is released with glutamate from synaptic vesicles upon neural excitation. Understanding the spatiotemporal regulation of mobile Zn[superscript 2+] at the synaptic level is challenging owing to the difficulty of visualizing Zn[superscript 2+] at individual synapses. Here we describe the use of zinc-responsive fluorescent probes together with two-photon microscopy to image Zn[superscript 2+] dynamics mediated by NMDA receptor-dependent long-term potentiation induction at single mossy fiber termini of dentate gyrus neurons in adult mouse hippocampal slices. The membrane-impermeant fluorescent Zn[superscript 2+] probe, 6-CO2H-ZAP4, was loaded into presynaptic vesicles in hippocampal mossy fiber termini upon KCl-induced depolarization, which triggers subsequent endocytosis and vesicular restoration. Local tetanic stimulation decreased the Zn[superscript 2+] signal observed at individual presynaptic sites, indicating release of the Zn[superscript 2+] from vesicles in synaptic potentiation. This synapse-level two-photon Zn[superscript 2+] imaging method enables monitoring of presynaptic Zn[superscript 2+] dynamics for improving the understanding of physiological roles of mobile Zn[superscript 2+] in regular and aberrant neurologic function.