---
APC_amount: 6248,82 EUR
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
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abstract:
- lang: eng
  text: It is widely believed that information storage in neuronal circuits involves
    nanoscopic structural changes at synapses, resulting in the formation of synaptic
    engrams. However, direct evidence for this hypothesis is lacking. To test this
    conjecture, we combined chemical potentiation, functional analysis by paired pre-postsynaptic
    recordings, and structural analysis by electron microscopy (EM) and freeze-fracture
    replica labeling (FRL) at the rodent hippocampal mossy fiber synapse, a key synapse
    in the trisynaptic circuit of the hippocampus. Biophysical analysis of synaptic
    transmission revealed that forskolin-induced chemical potentiation increased the
    readily releasable vesicle pool size and vesicular release probability by 146%
    and 49%, respectively. Structural analysis of mossy fiber synapses by EM and FRL
    demonstrated an increase in the number of vesicles close to the plasma membrane
    and the number of clusters of the priming protein Munc13-1, indicating an increase
    in the number of both docked and primed vesicles. Furthermore, FRL analysis revealed
    a significant reduction of the distance between Munc13-1 and CaV2.1 Ca2+ channels,
    suggesting reconfiguration of the channel-vesicle coupling nanotopography. Our
    results indicate that presynaptic plasticity is associated with structural reorganization
    of active zones. We propose that changes in potential nanoscopic organization
    at synaptic vesicle release sites may be correlates of learning and memory at
    a plastic central synapse.
acknowledged_ssus:
- _id: EM-Fac
- _id: PreCl
acknowledgement: "We thank Carolina Borges-Merjane, Jing-Jing Chen, Katharina Lichter,
  and Samuel Young for critically reading the manuscript; the Electron Microscopy
  Facility of ISTA, in particular Vanessa Zheden, for extensive support, advice, and
  experimental assistance; the Preclinical Facility of ISTA, in particular Victoria
  Wimmer and Michael Schunn, for experimental assistance; Florian Marr and Christina
  Altmutter for technical support; Alois Schlögl for help with analysis; and Eleftheria
  Kralli-Beller for manuscript editing. We also thank Cordelia Imig for providing
  Munc13-1cKO-Munc13-2/3(−/−) mutant mice. Part of the work has been published in
  O.K.’s thesis in partial fulfillment of the requirements for the degree of Doctor
  of Philosophy.\r\nThis project received funding from the European Research Council
  and European Union’s Horizon 2020 research and innovation programme (ERC 692692
  to P.J.; https://cordis.europa.eu/project/id/692692/de) and from the Fond zur Förderung
  der Wissenschaftlichen Forschung (Z312-B27 Wittgenstein award to P.J., https://www.fwf.ac.at/en/funding/portfolio/projects/fwf-wittgenstein-award;
  W1205-B09 and P36232-B to P.J., https://www.fwf.ac.at/en/funding; I6166-B to R.S.;
  https://www.fwf.ac.at/en/funding). The funders had no role in study design, data
  collection and analysis, decision to publish, or preparation of the manuscript."
article_number: e3002879
article_processing_charge: Yes
article_type: original
author:
- first_name: Olena
  full_name: Kim, Olena
  id: 3F8ABDDA-F248-11E8-B48F-1D18A9856A87
  last_name: Kim
  orcid: 0000-0003-2344-1039
- first_name: Yuji
  full_name: Okamoto, Yuji
  id: 3337E116-F248-11E8-B48F-1D18A9856A87
  last_name: Okamoto
  orcid: 0000-0003-0408-6094
- first_name: Walter
  full_name: Kaufmann, Walter
  id: 3F99E422-F248-11E8-B48F-1D18A9856A87
  last_name: Kaufmann
  orcid: 0000-0001-9735-5315
- first_name: Nils
  full_name: Brose, Nils
  last_name: Brose
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
citation:
  ama: Kim O, Okamoto Y, Kaufmann W, Brose N, Shigemoto R, Jonas PM. Presynaptic cAMP-PKA-mediated
    potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle
    coupling at hippocampal mossy fiber boutons. <i>PLoS Biology</i>. 2024;22(11).
    doi:<a href="https://doi.org/10.1371/journal.pbio.3002879">10.1371/journal.pbio.3002879</a>
  apa: Kim, O., Okamoto, Y., Kaufmann, W., Brose, N., Shigemoto, R., &#38; Jonas,
    P. M. (2024). Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration
    of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber
    boutons. <i>PLoS Biology</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pbio.3002879">https://doi.org/10.1371/journal.pbio.3002879</a>
  chicago: Kim, Olena, Yuji Okamoto, Walter Kaufmann, Nils Brose, Ryuichi Shigemoto,
    and Peter M Jonas. “Presynaptic CAMP-PKA-Mediated Potentiation Induces Reconfiguration
    of Synaptic Vesicle Pools and Channel-Vesicle Coupling at Hippocampal Mossy Fiber
    Boutons.” <i>PLoS Biology</i>. Public Library of Science, 2024. <a href="https://doi.org/10.1371/journal.pbio.3002879">https://doi.org/10.1371/journal.pbio.3002879</a>.
  ieee: O. Kim, Y. Okamoto, W. Kaufmann, N. Brose, R. Shigemoto, and P. M. Jonas,
    “Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic
    vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons,”
    <i>PLoS Biology</i>, vol. 22, no. 11. Public Library of Science, 2024.
  ista: Kim O, Okamoto Y, Kaufmann W, Brose N, Shigemoto R, Jonas PM. 2024. Presynaptic
    cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools
    and channel-vesicle coupling at hippocampal mossy fiber boutons. PLoS Biology.
    22(11), e3002879.
  mla: Kim, Olena, et al. “Presynaptic CAMP-PKA-Mediated Potentiation Induces Reconfiguration
    of Synaptic Vesicle Pools and Channel-Vesicle Coupling at Hippocampal Mossy Fiber
    Boutons.” <i>PLoS Biology</i>, vol. 22, no. 11, e3002879, Public Library of Science,
    2024, doi:<a href="https://doi.org/10.1371/journal.pbio.3002879">10.1371/journal.pbio.3002879</a>.
  short: O. Kim, Y. Okamoto, W. Kaufmann, N. Brose, R. Shigemoto, P.M. Jonas, PLoS
    Biology 22 (2024).
corr_author: '1'
date_created: 2024-12-01T23:01:54Z
date_published: 2024-11-18T00:00:00Z
date_updated: 2026-04-16T12:20:34Z
day: '18'
ddc:
- '570'
department:
- _id: PeJo
- _id: EM-Fac
- _id: RySh
doi: 10.1371/journal.pbio.3002879
ec_funded: 1
external_id:
  isi:
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  pmid:
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scopus_import: '1'
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title: Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic
  vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
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type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 22
year: '2024'
...
---
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_id: '11196'
abstract:
- lang: eng
  text: "One of the fundamental questions in Neuroscience is how the structure of
    synapses and their physiological properties are related. While synaptic transmission
    remains a dynamic process, electron microscopy provides images with comparably
    low temporal resolution (Studer et al., 2014). The current work overcomes this
    challenge and describes an improved “Flash and Freeze” technique (Watanabe et
    al., 2013a; Watanabe et al., 2013b) to study synaptic transmission at the hippocampal
    mossy fiber-CA3 pyramidal neuron synapses, using mouse acute brain slices and
    organotypic slices culture. The improved method allowed for selective stimulation
    of presynaptic mossy fiber boutons and the observation of synaptic vesicle pool
    dynamics at the active zones. Our results uncovered several intriguing morphological
    features of mossy fiber boutons. First, the docked vesicle pool was largely depleted
    (more than 70%) after stimulation, implying that the docked synaptic vesicles
    pool and readily releasable pool are vastly overlapping in mossy fiber boutons.
    Second, the synaptic vesicles are skewed towards larger diameters, displaying
    a wide range of sizes. An increase in the mean diameter of synaptic vesicles,
    after single and repetitive stimulation, suggests that smaller vesicles have a
    higher release probability. Third, we observed putative endocytotic structures
    after moderate light stimulation, matching the timing of previously described
    ultrafast endocytosis (Watanabe et al., 2013a; Delvendahl et al., 2016). \r\n\tIn
    addition, synaptic transmission depends on a sophisticated system of protein machinery
    and calcium channels (Südhof, 2013b), which amplifies the challenge in studying
    synaptic communication as these interactions can be potentially modified during
    synaptic plasticity. And although recent study elucidated the potential correlation
    between physiological and morphological properties of synapses during synaptic
    plasticity (Vandael et al., 2020), the molecular underpinning of it remains unknown.
    Thus, the presented work tries to overcome this challenge and aims to pinpoint
    changes in the molecular architecture at hippocampal mossy fiber bouton synapses
    during short- and long-term potentiation (STP and LTP), we combined chemical potentiation,
    with the application of a cyclic adenosine monophosphate agonist (i.e. forskolin)
    and freeze-fracture replica immunolabelling. This method allowed the localization
    of membrane-bound proteins with nanometer precision within the active zone, in
    particular, P/Q-type calcium channels and synaptic vesicle priming proteins Munc13-1/2.
    First, we found that the number of clusters of Munc13-1 in the mossy fiber bouton
    active zone increased significantly during STP, but decreased to lower than the
    control value during LTP. Secondly, although the distance between the calcium
    channels and Munc13-1s did not change after induction of STP, it shortened during
    the LTP phase. Additionally, forskolin did not affect Munc13-2 distribution during
    STP and LTP. These results indicate the existence of two distinct mechanisms that
    govern STP and LTP at mossy fiber bouton synapses: an increase in the readily
    realizable pool in the case of STP and a potential increase in release probability
    during LTP. “Flash and freeze” and functional electron microscopy, are versatile
    methods that can be successfully applied to intact brain circuits to study synaptic
    transmission even at the molecular level.\r\n"
acknowledged_ssus:
- _id: EM-Fac
- _id: PreCl
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Olena
  full_name: Kim, Olena
  id: 3F8ABDDA-F248-11E8-B48F-1D18A9856A87
  last_name: Kim
  orcid: 0000-0003-2344-1039
citation:
  ama: Kim O. Nanoarchitecture of hippocampal mossy fiber-CA3 pyramidal neuron synapses.
    2022. doi:<a href="https://doi.org/10.15479/at:ista:11196">10.15479/at:ista:11196</a>
  apa: Kim, O. (2022). <i>Nanoarchitecture of hippocampal mossy fiber-CA3 pyramidal
    neuron synapses</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:11196">https://doi.org/10.15479/at:ista:11196</a>
  chicago: Kim, Olena. “Nanoarchitecture of Hippocampal Mossy Fiber-CA3 Pyramidal
    Neuron Synapses.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11196">https://doi.org/10.15479/at:ista:11196</a>.
  ieee: O. Kim, “Nanoarchitecture of hippocampal mossy fiber-CA3 pyramidal neuron
    synapses,” Institute of Science and Technology Austria, 2022.
  ista: Kim O. 2022. Nanoarchitecture of hippocampal mossy fiber-CA3 pyramidal neuron
    synapses. Institute of Science and Technology Austria.
  mla: Kim, Olena. <i>Nanoarchitecture of Hippocampal Mossy Fiber-CA3 Pyramidal Neuron
    Synapses</i>. Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11196">10.15479/at:ista:11196</a>.
  short: O. Kim, Nanoarchitecture of Hippocampal Mossy Fiber-CA3 Pyramidal Neuron
    Synapses, Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-04-20T09:47:12Z
date_published: 2022-04-20T00:00:00Z
date_updated: 2026-06-18T10:49:27Z
day: '20'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: PeJo
- _id: GradSch
doi: 10.15479/at:ista:11196
ec_funded: 1
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project:
- _id: 25BAF7B2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '708497'
  name: Presynaptic calcium channels distribution and impact on coupling at the hippocampal
    mossy fiber synapse
- _id: 25B7EB9E-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '692692'
  name: Biophysics and circuit function of a giant cortical glutamatergic synapse
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  call_identifier: FWF
  grant_number: Z00312
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publication_identifier:
  issn:
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publisher: Institute of Science and Technology Austria
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supervisor:
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  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
title: Nanoarchitecture of hippocampal mossy fiber-CA3 pyramidal neuron synapses
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  short: CC BY-NC-ND (4.0)
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...
---
_id: '7473'
abstract:
- lang: eng
  text: How structural and functional properties of synapses relate to each other
    is a fundamental question in neuroscience. Electrophysiology has elucidated mechanisms
    of synaptic transmission, and electron microscopy (EM) has provided insight into
    morphological properties of synapses. Here we describe an enhanced method for
    functional EM (“flash and freeze”), combining optogenetic stimulation with high-pressure
    freezing. We demonstrate that the improved method can be applied to intact networks
    in acute brain slices and organotypic slice cultures from mice. As a proof of
    concept, we probed vesicle pool changes during synaptic transmission at the hippocampal
    mossy fiber-CA3 pyramidal neuron synapse. Our findings show overlap of the docked
    vesicle pool and the functionally defined readily releasable pool and provide
    evidence of fast endocytosis at this synapse. Functional EM with acute slices
    and slice cultures has the potential to reveal the structural and functional mechanisms
    of transmission in intact, genetically perturbed, and disease-affected synapses.
acknowledgement: This project has received funding from the European Research Council
  (ERC) and European Commission (EC), under the European Union’s Horizon 2020 research
  and innovation programme (ERC grant agreement No. 692692 and Marie Sklodowska-Curie
  708497) and from Fonds zur Förderung der Wissenschaftlichen Forschung (Z 312-B27
  Wittgenstein award and DK W1205-B09). We thank Johann Danzl and Ryuichi Shigemoto
  for critically reading the manuscript; Walter Kaufmann, Daniel Gutl, and Vanessa
  Zheden for extensive EM training, advice, and experimental assistance; Benjamin
  Suter for substantial help with light stimulation, ImageJ plugins for analysis,
  and manuscript editing; Florian Marr and Christina Altmutter for technical support;
  Eleftheria Kralli-Beller for manuscript editing; Julia König and Paul Wurzinger
  (Leica Microsystems) for helpful technical discussions; and Taija Makinen for providing
  the Prox1-CreERT2 mouse line.
article_processing_charge: No
article_type: original
author:
- first_name: Carolina
  full_name: Borges Merjane, Carolina
  id: 4305C450-F248-11E8-B48F-1D18A9856A87
  last_name: Borges Merjane
  orcid: 0000-0003-0005-401X
- first_name: Olena
  full_name: Kim, Olena
  id: 3F8ABDDA-F248-11E8-B48F-1D18A9856A87
  last_name: Kim
  orcid: 0000-0003-2344-1039
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
citation:
  ama: Borges Merjane C, Kim O, Jonas PM. Functional electron microscopy (“Flash and
    Freeze”) of identified cortical synapses in acute brain slices. <i>Neuron</i>.
    2020;105:992-1006. doi:<a href="https://doi.org/10.1016/j.neuron.2019.12.022">10.1016/j.neuron.2019.12.022</a>
  apa: Borges Merjane, C., Kim, O., &#38; Jonas, P. M. (2020). Functional electron
    microscopy (“Flash and Freeze”) of identified cortical synapses in acute brain
    slices. <i>Neuron</i>. Elsevier. <a href="https://doi.org/10.1016/j.neuron.2019.12.022">https://doi.org/10.1016/j.neuron.2019.12.022</a>
  chicago: Borges Merjane, Carolina, Olena Kim, and Peter M Jonas. “Functional Electron
    Microscopy (‘Flash and Freeze’) of Identified Cortical Synapses in Acute Brain
    Slices.” <i>Neuron</i>. Elsevier, 2020. <a href="https://doi.org/10.1016/j.neuron.2019.12.022">https://doi.org/10.1016/j.neuron.2019.12.022</a>.
  ieee: C. Borges Merjane, O. Kim, and P. M. Jonas, “Functional electron microscopy
    (‘Flash and Freeze’) of identified cortical synapses in acute brain slices,” <i>Neuron</i>,
    vol. 105. Elsevier, pp. 992–1006, 2020.
  ista: Borges Merjane C, Kim O, Jonas PM. 2020. Functional electron microscopy (“Flash
    and Freeze”) of identified cortical synapses in acute brain slices. Neuron. 105,
    992–1006.
  mla: Borges Merjane, Carolina, et al. “Functional Electron Microscopy (‘Flash and
    Freeze’) of Identified Cortical Synapses in Acute Brain Slices.” <i>Neuron</i>,
    vol. 105, Elsevier, 2020, pp. 992–1006, doi:<a href="https://doi.org/10.1016/j.neuron.2019.12.022">10.1016/j.neuron.2019.12.022</a>.
  short: C. Borges Merjane, O. Kim, P.M. Jonas, Neuron 105 (2020) 992–1006.
corr_author: '1'
date_created: 2020-02-10T15:59:45Z
date_published: 2020-03-18T00:00:00Z
date_updated: 2026-09-10T22:30:04Z
day: '18'
ddc:
- '570'
department:
- _id: PeJo
doi: 10.1016/j.neuron.2019.12.022
ec_funded: 1
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  - '000520854700008'
  pmid:
  - '31928842'
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  name: Biophysics and circuit function of a giant cortical glutamatergic synapse
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  call_identifier: FWF
  grant_number: W01205
  name: Zellkommunikation in Gesundheit und Krankheit
publication: Neuron
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  issn:
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publisher: Elsevier
quality_controlled: '1'
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title: Functional electron microscopy (“Flash and Freeze”) of identified cortical
  synapses in acute brain slices
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  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 105
year: '2020'
...
---
_id: '11222'
acknowledgement: This work was supported by the ERC and EU Horizon 2020 (ERC 692692;
  MSC-IF 708497) and FWF Z 312-B27 Wittgenstein award; W 1205-B09).
article_number: A3.27
article_processing_charge: No
author:
- first_name: Olena
  full_name: Kim, Olena
  id: 3F8ABDDA-F248-11E8-B48F-1D18A9856A87
  last_name: Kim
  orcid: 0000-0003-2344-1039
- first_name: Carolina
  full_name: Borges Merjane, Carolina
  id: 4305C450-F248-11E8-B48F-1D18A9856A87
  last_name: Borges Merjane
  orcid: 0000-0003-0005-401X
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
citation:
  ama: 'Kim O, Borges Merjane C, Jonas PM. Functional analysis of the docked vesicle
    pool in hippocampal mossy fiber terminals by electron microscopy. In: <i>Intrinsic
    Activity</i>. Vol 7. Austrian Pharmacological Society; 2019. doi:<a href="https://doi.org/10.25006/ia.7.s1-a3.27">10.25006/ia.7.s1-a3.27</a>'
  apa: 'Kim, O., Borges Merjane, C., &#38; Jonas, P. M. (2019). Functional analysis
    of the docked vesicle pool in hippocampal mossy fiber terminals by electron microscopy.
    In <i>Intrinsic Activity</i> (Vol. 7). Innsbruck, Austria: Austrian Pharmacological
    Society. <a href="https://doi.org/10.25006/ia.7.s1-a3.27">https://doi.org/10.25006/ia.7.s1-a3.27</a>'
  chicago: Kim, Olena, Carolina Borges Merjane, and Peter M Jonas. “Functional Analysis
    of the Docked Vesicle Pool in Hippocampal Mossy Fiber Terminals by Electron Microscopy.”
    In <i>Intrinsic Activity</i>, Vol. 7. Austrian Pharmacological Society, 2019.
    <a href="https://doi.org/10.25006/ia.7.s1-a3.27">https://doi.org/10.25006/ia.7.s1-a3.27</a>.
  ieee: O. Kim, C. Borges Merjane, and P. M. Jonas, “Functional analysis of the docked
    vesicle pool in hippocampal mossy fiber terminals by electron microscopy,” in
    <i>Intrinsic Activity</i>, Innsbruck, Austria, 2019, vol. 7, no. Suppl. 1.
  ista: 'Kim O, Borges Merjane C, Jonas PM. 2019. Functional analysis of the docked
    vesicle pool in hippocampal mossy fiber terminals by electron microscopy. Intrinsic
    Activity. ANA: Austrian Neuroscience Association ; APHAR: Austrian Pharmacological
    Society vol. 7, A3.27.'
  mla: Kim, Olena, et al. “Functional Analysis of the Docked Vesicle Pool in Hippocampal
    Mossy Fiber Terminals by Electron Microscopy.” <i>Intrinsic Activity</i>, vol.
    7, no. Suppl. 1, A3.27, Austrian Pharmacological Society, 2019, doi:<a href="https://doi.org/10.25006/ia.7.s1-a3.27">10.25006/ia.7.s1-a3.27</a>.
  short: O. Kim, C. Borges Merjane, P.M. Jonas, in:, Intrinsic Activity, Austrian
    Pharmacological Society, 2019.
conference:
  end_date: 2019-09-27
  location: Innsbruck, Austria
  name: 'ANA: Austrian Neuroscience Association ; APHAR: Austrian Pharmacological
    Society'
  start_date: 2019-09-25
corr_author: '1'
date_created: 2022-04-20T15:06:05Z
date_published: 2019-09-11T00:00:00Z
date_updated: 2026-09-10T22:30:04Z
day: '11'
ddc:
- '570'
department:
- _id: PeJo
doi: 10.25006/ia.7.s1-a3.27
ec_funded: 1
fulldoi: https://doi.org/10.25006/ia.7.s1-a3.27
intvolume: '         7'
issue: Suppl. 1
keyword:
- hippocampus
- mossy fibers
- readily releasable pool
- electron microscopy
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.intrinsicactivity.org/2019/7/S1/A3.27/
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: 25B7EB9E-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '692692'
  name: Biophysics and circuit function of a giant cortical glutamatergic synapse
- _id: 25BAF7B2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '708497'
  name: Presynaptic calcium channels distribution and impact on coupling at the hippocampal
    mossy fiber synapse
- _id: 25C3DBB6-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W01205
  name: Zellkommunikation in Gesundheit und Krankheit
- _id: 25C5A090-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z00312
  name: Synaptic communication in neuronal microcircuits
publication: Intrinsic Activity
publication_identifier:
  issn:
  - 2309-8503
publication_status: published
publisher: Austrian Pharmacological Society
quality_controlled: '1'
related_material:
  record:
  - id: '11196'
    relation: dissertation_contains
    status: public
status: public
title: Functional analysis of the docked vesicle pool in hippocampal mossy fiber terminals
  by electron microscopy
type: conference_abstract
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2019'
...
