Evidence map›Paper›PMID 32989096›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2020

Release Mode Dynamically Regulates the RRP Refilling Mechanism at Individual Hippocampal Synapses.

Yujin Kim, Unghwi Lee, Chunghon Choi, Sunghoe Chang

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. The SphK1/S1P Axis Regulates Synaptic Vesicle Endocytosis via TRPC5 Channels.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yujin KimDepartment of Physiology and Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea 03080, and Neuroscience Research Institute, Medical Research Center, Seoul National University College of Medicine, Seoul, South Korea, 03080.
Unghwi LeeDepartment of Physiology and Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea 03080, and Neuroscience Research Institute, Medical Research Center, Seoul National University College of Medicine, Seoul, South Korea, 03080.ORCID 0000-0002-9956-7570
Chunghon ChoiDepartment of Physiology and Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea 03080, and Neuroscience Research Institute, Medical Research Center, Seoul National University College of Medicine, Seoul, South Korea, 03080.ORCID 0000-0002-9250-2651
Sunghoe ChangDepartment of Physiology and Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea 03080, and Neuroscience Research Institute, Medical Research Center, Seoul National University College of Medicine, Seoul, South Korea, 03080 sunghoe@snu.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synaptic strength and reliability are determined by the number of vesicles released per action potential and the availability of release-competent vesicles in the readily releasable pool (RRP). Compared with release of a single vesicle (univesicular release), multivesicular release (MVR) would speed up RRP depletion, yet whether the RRP is refilled differently during the two different release modes has not been investigated. Here, we address this question by quantitative optical imaging with an axon-targeting glutamate sensor, iGluSnFRpre. We found that hippocampal synapses preferentially release multiple vesicles per action potential at high extracellular calcium or by paired-pulse stimulation. When MVR prevails, the RRP is recovered very rapidly with a time constant of 430 ms. This rapid recovery is mediated by dynamin-dependent endocytosis followed by direct reuse of retrieved vesicles. Furthermore, our simulation proved that the portion of retrieved vesicles that directly refill the RRP increases dramatically (>70%) in MVR compared with that in univesicular release (<10%). These results suggest that the contribution of rapid and direct recruitment of retrieved vesicle to the RRP changes dynamically with release mode at the level of individual synapses, which suggests a form of presynaptic homeostatic plasticity for reliable synaptic transmission during various synaptic activity.

Indexed as

Action PotentialsAnimalsAxonsCalcium SignalingComputer SimulationDynaminsElectrophysiological PhenomenaEndocytosisGlutamic AcidHippocampusImmunohistochemistryKineticsRatsSynapsesSynaptic TransmissionSynaptic VesiclesDynaminsGlutamic Acidhippocampal synapse homeostatic mechanismmultivesicular releaseRRP replenishmentsynaptic vesicle reuse

Identifiers

PMID32989096
PMCPMC7605427

What OpenQuestion holds

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Registered trials

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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.