Evidence map›Paper›PMID 32228859›Full record

ArticleeLife2020

Incomplete vesicular docking limits synaptic strength under high release probability conditions.

Gerardo Malagon, Takafumi Miki, Van Tran, Laura C Gomez, Alain Marty

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  5. Review
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  11. Fully-primed slowly-recovering vesicles mediate presynaptic LTP at neocortical neurons.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Forty years of the adrenal chromaffin cell through ISCCB meetings around the world.Pflugers Archiv : European journal of physiology · 2023
    Review
  13. Article
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  15. Article
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  18. Review
  19. Stochastic Properties of Spontaneous Synaptic Transmission at Individual Active Zones.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  20. Three small vesicular pools in sequence govern synaptic response dynamics during action potential trains.Proceedings of the National Academy of Sciences of the United States of America · 2022
    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

5 authors at 1 institution in 3 countries.

Gerardo MalagonUniversité de Paris, SPPIN-Saints Pères Paris Institute for the Neurosciences, CNRS, Paris, France.
Takafumi MikiUniversité de Paris, SPPIN-Saints Pères Paris Institute for the Neurosciences, CNRS, Paris, France.
Van TranUniversité de Paris, SPPIN-Saints Pères Paris Institute for the Neurosciences, CNRS, Paris, France.
Laura C GomezUniversité de Paris, SPPIN-Saints Pères Paris Institute for the Neurosciences, CNRS, Paris, France.
Alain MartyUniversité de Paris, SPPIN-Saints Pères Paris Institute for the Neurosciences, CNRS, Paris, France.ORCID 0000-0001-6478-6880
Centre National de la Recherche Scientifique · FR

Funding

Centre National de la Recherche Scientifique UMR 8003Fondation pour la Recherche Médicale SPF201809007190H2020 European Research Council 294509JSPS JP18K06472
6 · The paper itself

Abstract

Central mammalian synapses release synaptic vesicles in dedicated structures called docking/release sites. It has been assumed that when voltage-dependent calcium entry is sufficiently large, synaptic output attains a maximum value of one synaptic vesicle per action potential and per site. Here we use deconvolution to count synaptic vesicle output at single sites (mean site number per synapse: 3.6). When increasing calcium entry with tetraethylammonium in 1.5 mM external calcium concentration, we find that synaptic output saturates at 0.22 vesicle per site, not at 1 vesicle per site. Fitting the results with current models of calcium-dependent exocytosis indicates that the 0.22 vesicle limit reflects the probability of docking sites to be occupied by synaptic vesicles at rest, as only docked vesicles can be released. With 3 mM external calcium, the maximum output per site increases to 0.47, indicating an increase in docking site occupancy as a function of external calcium concentration.

Indexed as

Action PotentialsAnimalsCalciumExocytosisProbabilityRatsRats, Sprague-DawleySynaptic TransmissionSynaptic VesiclesTetraethylammoniumCalciumTetraethylammoniumcalcium concentrationneuroscienceratrelease sitesynapse

Identifiers

PMID32228859
PMCPMC7136020
OpenAlexW3012995667

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.