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Articles, Cellular/Molecular

Synaptically Released Zinc Triggers Metabotropic Signaling via a Zinc-Sensing Receptor in the Hippocampus

Limor Besser, Ehud Chorin, Israel Sekler, William F. Silverman, Stan Atkin, James T. Russell and Michal Hershfinkel
Journal of Neuroscience 4 March 2009, 29 (9) 2890-2901; DOI: https://doi.org/10.1523/JNEUROSCI.5093-08.2009
Limor Besser
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Ehud Chorin
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Israel Sekler
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William F. Silverman
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Stan Atkin
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James T. Russell
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Michal Hershfinkel
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Abstract

Zn2+ is coreleased with glutamate from mossy fiber terminals and can influence synaptic function. Here, we demonstrate that synaptically released Zn2+ activates a selective postsynaptic Zn2+-sensing receptor (ZnR) in the CA3 region of the hippocampus. ZnR activation induced intracellular release of Ca2+, as well as phosphorylation of extracellular-regulated kinase and Ca2+/calmodulin kinase II. Blockade of synaptic transmission by tetrodotoxin or CdCl inhibited the ZnR-mediated Ca2+ rises. The responses mediated by ZnR were largely attenuated by the extracellular Zn2+ chelator, CaEDTA, and in slices from mice lacking vesicular Zn2+, suggesting that synaptically released Zn2+ triggers the metabotropic activity. Knockdown of the expression of the orphan G-protein-coupled receptor 39 (GPR39) attenuated ZnR activity in a neuronal cell line. Importantly, we observed widespread GPR39 labeling in CA3 neurons, suggesting a role for this receptor in mediating ZnR signaling in the hippocampus. Our results describe a unique role for synaptic Zn2+ acting as the physiological ligand of a metabotropic receptor and provide a novel pathway by which synaptic Zn2+ can regulate neuronal function.

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The Journal of Neuroscience: 29 (9)
Journal of Neuroscience
Vol. 29, Issue 9
4 Mar 2009
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Synaptically Released Zinc Triggers Metabotropic Signaling via a Zinc-Sensing Receptor in the Hippocampus
Limor Besser, Ehud Chorin, Israel Sekler, William F. Silverman, Stan Atkin, James T. Russell, Michal Hershfinkel
Journal of Neuroscience 4 March 2009, 29 (9) 2890-2901; DOI: 10.1523/JNEUROSCI.5093-08.2009

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Synaptically Released Zinc Triggers Metabotropic Signaling via a Zinc-Sensing Receptor in the Hippocampus
Limor Besser, Ehud Chorin, Israel Sekler, William F. Silverman, Stan Atkin, James T. Russell, Michal Hershfinkel
Journal of Neuroscience 4 March 2009, 29 (9) 2890-2901; DOI: 10.1523/JNEUROSCI.5093-08.2009
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  • Re: The Origin of Zinc
    Michal Hershfinkel
    Published on: 29 March 2009
  • The Origin of Zinc
    Katalin Toth
    Published on: 16 March 2009
  • Published on: (29 March 2009)
    Page navigation anchor for Re: The Origin of Zinc
    Re: The Origin of Zinc
    • Michal Hershfinkel, Researcher

    The hypothesis that the free-Zn2+ contained in synaptic vesicles is co-released with glutamate has been evaluated and confirmed by numerous studies using a variety of approaches; from earlier work using 65Zn or atomic absorption spectrometry (Assaf and Chung, 1984; Howell et al., 1984; Aniksztejn et al., 1987), to more recent studies in which Zn2+- sensitive fluorescent dyes were employed (Thompson et al., 2000; Li et a...

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    The hypothesis that the free-Zn2+ contained in synaptic vesicles is co-released with glutamate has been evaluated and confirmed by numerous studies using a variety of approaches; from earlier work using 65Zn or atomic absorption spectrometry (Assaf and Chung, 1984; Howell et al., 1984; Aniksztejn et al., 1987), to more recent studies in which Zn2+- sensitive fluorescent dyes were employed (Thompson et al., 2000; Li et al., 2001; Ueno et al., 2002; Qian and Noebels, 2005; Frederickson et al., 2006).

    Of particular note and significance to our work, Qian and Noebels (2005) elegantly demonstrated that Zn2+ rise is detected with the glutamate release following mossy fiber (MF) stimulation. Importantly, they showed that synaptic Zn2+ is a cotransmitter released with glutamate under physiological conditions. This directly attests to the relevance of this process in neuronal signaling in the CA3 region. Our results demonstrate, for the first time, a unique target for synaptically Zn2+, the ZnR, which is activated following MF stimulation. Additionally, we identified a molecular moiety, GPR39, that putatively mediates ZnR signaling.

    1. The studies cited by Toth focus on the response of single neurons using approaches appropriate for the aims of those studies. In contrast, we employed bulk loading of the Ca2+-sensitive dye Fura-2, in order to monitor cytoplasmic Ca2+ signals in populations of neurons (Beierlein et al., 2002). As a result, we show prolonged signals representing the average of many cells, responding at slightly different times. Application of an agonist of the group I mGluR induced a Ca2+ response similar to that triggered by Zn2+.

    The metabotropic nature of the ZnR response is strongly supported by the controls we used, among them, depletion of intracellular Ca2+ stores as well as the Gq and PLC inhibitors. Therefore, the most likely mechanism for the observed Zn2+-dependent signaling is a metabotropic Gq-coupled receptor.

    2. The Ca2+ response is the delta of the peak from the baseline obtained prior to stimulation. In ZnT3 KO mice, Fig. 7E, this response was approximately 50% of that obtained in WT mice, Fig. 7C. The average of the responses is shown in the bar graph of Fig. 7F in which the scale differs from that of Fig. 7D.

    3. Attenuation of the Ca2+ signal in the ZnT3 KO mice, or following application of the extracellular Zn2+ chelator in WT animals, indicates that the metabotropic signaling is largely mediated by synaptically- released Zn2+, demonstrated to occur within and to be released from the mossy fibers. The protocol we employed to trigger this release is well established (Qian and Noebels, 2005). Thus, the possibility that other pathways might have been activated in our system in no way alters the conclusion that synaptic Zn2+ induces the ZnR-metabotropic response in CA3 neurons.

    Aniksztejn L, Charton G, Ben-Ari Y (1987) Selective release of endogenous zinc from the hippocampal mossy fibers in situ. Brain Res 404:58-64.

    Assaf SY, Chung SH (1984) Release of endogenous Zn2+ from brain tissue during activity. Nature 308:734-736.

    Beierlein M, Fall CP, Rinzel J, Yuste R (2002) Thalamocortical bursts trigger recurrent activity in neocortical networks: layer 4 as a frequency -dependent gate. J Neurosci 22:9885-9894.

    Frederickson CJ, Giblin LJ, 3rd, Balaji RV, Masalha R, Frederickson CJ, Zeng Y, Lopez EV, Koh JY, Chorin U, Besser L, Hershfinkel M, Li Y, Thompson RB, Krezel A (2006) Synaptic release of zinc from brain slices: factors governing release, imaging, and accurate calculation of concentration. J Neurosci Methods 154:19-29. .

    Howell GA, Welch MG, Frederickson CJ (1984) Stimulation-induced uptake and release of zinc in hippocampal slices. Nature 308:736-738

    Li Y, Hough CJ, Suh SW, Sarvey JM, Frederickson CJ (2001) Rapid translocation of Zn(2+) from presynaptic terminals into postsynaptic hippocampal neurons after physiological stimulation. J Neurophysiol 86:2597-2604.

    Qian J, Noebels JL (2005) Visualization of transmitter release with zinc fluorescence detection at the mouse hippocampal mossy fibre synapse. J Physiol 566:747-758.

    Thompson RB, Whetsell WOJ, Maliwal BP, Fierke CA, Frederickson CJ (2000) Fluorescence microscopy of stimulated Zn(II) release from organotypic cultures of mammalian hippocampus using a carbonic anhydrase- based biosensor system. J Neurosci Methods 96:35-45.

    Ueno S, Tsukamoto M, Hirano T, Kikuchi K, Yamada MK, Nishiyama N, Nagano T, Matsuki N, Ikegaya Y (2002) Mossy fiber Zn2+ spillover modulates heterosynaptic N-methyl-D-aspartate receptor activity in hippocampal CA3 circuits. J Cell Biol 158:215-220.

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    Competing Interests: None declared.
  • Published on: (16 March 2009)
    Page navigation anchor for The Origin of Zinc
    The Origin of Zinc
    • Katalin Toth, Associate Professor

    In Besser et al. (2009) the authors claim that synaptically released zinc triggers metabotropic responses in the hippocampus. However, whether zinc is in fact released from synaptic vesicles remains equivocal (Kay and Tóth, 2008; Paoletti et al., 2009). Due to this contentious issue it is crucial to design and execute experiments that provide definitive proof of the origin of zinc responsible for the effects observed...

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    In Besser et al. (2009) the authors claim that synaptically released zinc triggers metabotropic responses in the hippocampus. However, whether zinc is in fact released from synaptic vesicles remains equivocal (Kay and Tóth, 2008; Paoletti et al., 2009). Due to this contentious issue it is crucial to design and execute experiments that provide definitive proof of the origin of zinc responsible for the effects observed by the authors. There are several important issues that should be addressed to validate the authors’ interpretation that their results relate to zinc released from synaptic vesicles.

    1. Ca2+ signals measured in CA3 pyramidal cells do not return to baseline values after the stimulus within the time frame examined. This puzzling observation stands in contrast to previously published data (Miller et al., 1996; Yeckel et al., 1999; Kapur et al., 2001) and may relate to the use of a cell-permeable Ca2+ dye. Previous studies used cell-impermeable dye delivered through a patch pipette to monitor Ca2+ signals in individual CA3 pyramidal cells. Cell-permeable Ca2+ indicators permeate membranes of intracellular organelles where they tend to accumulate (Connor, 1993; Gerasimenko and Tepikin, 2005), therefore fluorescent measurements might reflect signals originating from these cellular elements obscuring signals related to Ca2+ release.

    2. Despite strikingly similar Ca2+ signals in wild-type and ZnT3 KO animals the authors claim that responses in KO tissue are significantly decreased. However, when ZnT3 KO traces from Fig. 7E are scaled to Fig 7C, there is no obvious difference between Ca2+ responses from KO and WT.

    3. Mossy fibre inputs have not been identified pharmacologically or by any other criteria, generally used for experiments aiming to selectively activate mossy fibre inputs (Yeckel et al., 1999; Huang et al., 2008; Castillo et al., 1997; Toth et al., 2000). In a single slice the authors see responses in 23-26 CA3 pyramidal cells after bulk stimulation in the dentate gyrus. Such stimulation undoubtedly activates multiple fibres which can lead to polysynaptic recruitment of the CA3 auto-associative network. Such polysynaptic contamination combined with the long response delay makes it is impossible to conclude with any certainty that the Ca2+ signals observed result directly from mossy fibre activation.

    Castillo PE, Janz R, Südhof TC, Tzounopoulos T, Malenka RC, Nicoll RA (1997) Rab3A is essential for mossy fibre long-term potentiation in the hippocampus. Nature 388:590-593.

    Connor JA (1993) Intracellular calcium mobilization by inositol 1,4,5 - trisphosphate: intracellular movements and compartmentalization. Cell Calcium 14:185-200.

    Gerasimenko O, Tepikin A (2005) How to measure Ca2+ in cellular organelles? Cell Calcium 38:201-211.

    Huang YZ, Pan E, Xiong ZQ, McNamara JO (2008) Zinc-mediated transactivation of TrkB potentiates the hippocampal mossy fiber-CA3 pyramid synapse. Neuron 57:546-558.

    Kapur A, Yeckel M, Johnston D (2001) Hippocampal mossy fiber activity evokes Ca2+ release in CA3 pyramidal neurons via a metabotropic glutamate receptor pathway. Neuroscience 107:59-69.

    Kay AR, Tóth K (2008) Is zinc a neuromodulator? Sci Signal 1:re3. Miller LD, Petrozzino JJ, Golarai G, Connor JA (1996) Ca2+ release from intracellular stores induced by afferent stimulation of CA3 pyramidal neurons in hippocampal slices. J Neurophysiol 76:554-562.

    Paoletti P, Vergnano AM, Barbour B, Casado M (2009) Zinc at glutamatergic synapses. Neuroscience 158:126-136.

    Toth K, Suares G, Lawrence JJ, Philips-Tansey E, McBain CJ (2000) Differential mechanisms of transmission at three types of mossy fiber synapse. J Neurosci 20:8279-8289.

    Yeckel MF, Kapur A, Johnston D (1999) Multiple forms of LTP in hippocampal CA3 neurons use a common postsynaptic mechanism. Nat Neurosci 2:625- 633.

    Show Less
    Competing Interests: None declared.

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