Evidence map›Paper›PMID 25199706›Full record

ArticleNeuron2014

Uniquantal release through a dynamic fusion pore is a candidate mechanism of hair cell exocytosis.

Nikolai M Chapochnikov, Hideki Takago, Chao-Hua Huang, Tina Pangršič, Darina Khimich, Jakob Neef, Elisabeth Auge, Fabian Göttfert, Stefan W Hell, Carolin Wichmann and 2 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Neuron, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

54 citing papers in PubMed, 110 citations in OpenAlex.

  1. High-Pressure Freezing EM Tomography of Entire Ribbon Synapses in the Retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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  7. Auditory hair cells and spiral ganglion neurons regenerate synapses with refined release properties in vitro.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  8. CaProceedings of the National Academy of Sciences of the United States of America · 2023
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  13. The Impact of Multivesicular Release on the Transmission of Sensory Information by Ribbon Synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Nikolai M ChapochnikovInnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, 37075 Göttingen, Germany; Bernstein Center for Computational Neuroscience, University of Göttingen, 37073 Göttingen, Germany; Max Planck Institute for Dynamics and Self-Organization, 37077 Göttingen, Germany.
Hideki TakagoInnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, 37075 Göttingen, Germany; Department of Rehabilitation for Sensory Functions, Research Institute, National Rehabilitation Center for Persons with Disabilities, Saitama 359-8555, Japan.
Chao-Hua HuangInnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, 37075 Göttingen, Germany; Collaborative Research Center 889 Cellular Mechanisms of Sensory Processing, 37099 Göttingen, Germany.
Tina PangršičInnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, 37075 Göttingen, Germany; Collaborative Research Center 889 Cellular Mechanisms of Sensory Processing, 37099 Göttingen, Germany.
Darina KhimichInnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Jakob NeefInnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, 37075 Göttingen, Germany; Collaborative Research Center 889 Cellular Mechanisms of Sensory Processing, 37099 Göttingen, Germany.
Elisabeth AugeInnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, 37075 Göttingen, Germany; Molecular Architecture of Synapses Junior Research Group, University Medical Center Göttingen, 37075 Göttingen, Germany.
Fabian GöttfertDepartment of Nanobiophotonics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
Stefan W HellDepartment of Nanobiophotonics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany; Center for Nanoscale Microscopy and Molecular Physiology of the Brain, University of Göttingen, 37073 Göttingen, Germany.
Carolin WichmannInnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, 37075 Göttingen, Germany; Collaborative Research Center 889 Cellular Mechanisms of Sensory Processing, 37099 Göttingen, Germany; Molecular Architecture of Synapses Junior Research Group, University Medical Center Göttingen, 37075 Göttingen, Germany. Electronic address: cwichma@gwdg.de.
Fred WolfBernstein Center for Computational Neuroscience, University of Göttingen, 37073 Göttingen, Germany; Max Planck Institute for Dynamics and Self-Organization, 37077 Göttingen, Germany; Collaborative Research Center 889 Cellular Mechanisms of Sensory Processing, 37099 Göttingen, Germany. Electronic address: fred@nld.ds.mpg.de.
Tobias MoserInnerEarLab, Department of Otolaryngology, University Medical Center Göttingen, 37075 Göttingen, Germany; Bernstein Center for Computational Neuroscience, University of Göttingen, 37073 Göttingen, Germany; Collaborative Research Center 889 Cellular Mechanisms of Sensory Processing, 37099 Göttingen, Germany; Center for Nanoscale Microscopy and Molecular Physiology of the Brain, University of Göttingen, 37073 Göttingen, Germany. Electronic address: tmoser@gwdg.de.
Max Planck Institute for Biophysical Chemistry · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanisms underlying the large amplitudes and heterogeneity of excitatory postsynaptic currents (EPSCs) at inner hair cell (IHC) ribbon synapses are unknown. Based on electrophysiology, electron and superresolution light microscopy, and modeling, we propose that uniquantal exocytosis shaped by a dynamic fusion pore is a candidate neurotransmitter release mechanism in IHCs. Modeling indicated that the extended postsynaptic AMPA receptor clusters enable large uniquantal EPSCs. Recorded multiphasic EPSCs were triggered by similar glutamate amounts as monophasic ones and were consistent with progressive vesicle emptying during pore flickering. The fraction of multiphasic EPSCs decreased in absence of Ca(2+) influx and upon application of the Ca(2+) channel modulator BayK8644. Our experiments and modeling did not support the two most popular multiquantal release interpretations of EPSC heterogeneity: (1) Ca(2+)-synchronized exocytosis of multiple vesicles and (2) compound exocytosis fueled by vesicle-to-vesicle fusion. We propose that IHC synapses efficiently use uniquantal glutamate release for achieving high information transmission rates.

Indexed as

ExocytosisModels, NeurologicalAnimalsExcitatory Postsynaptic PotentialsHair Cells, Auditory, InnerMiceMice, Inbred C57BLModels, TheoreticalNeurotransmitter AgentsPatch-Clamp TechniquesRatsRats, WistarSynaptic TransmissionNeurotransmitter Agents

Identifiers

PMID25199706
OpenAlexW2028938372

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.