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...
Main Authors: | , , , , , , , |
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Other Authors: | |
Format: | Article |
Language: | en_US |
Published: |
National Academy of Sciences (U.S.)
2014
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Online Access: | http://hdl.handle.net/1721.1/91965 https://orcid.org/0000-0002-2693-4982 |
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. |
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