Evidence map›Paper›PMID 31364987›Full record

ArticleeLife2019

The readily-releasable pool dynamically regulates multivesicular release.

Jada H Vaden, Gokulakrishna Banumurthy, Eugeny S Gusarevich, Linda Overstreet-Wadiche, Jacques I Wadiche

Abstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Article
  2. Alzheimer's Pathology Enhances Excitatory Synaptic Input and Integration in VTA Dopamine Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Review
  4. Pathway-Specific Ultrastructure of Thalamocortical Synapses in Mouse Somatosensory Area S2.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Glycine Release Is Potentiated by cAMP via EPAC2 and CaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  20. 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.

Jada H VadenDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.ORCID 0000-0002-1295-0236
Gokulakrishna BanumurthyDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
Eugeny S GusarevichDepartment of Fundamental and Applied Physics, Northern (Arctic) Federal University named after M.V. Lomonosov, Arkhangelsk, Russian Federation.ORCID 0000-0002-8642-6293
Linda Overstreet-WadicheDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.ORCID 0000-0001-7367-5998
Jacques I WadicheDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.ORCID 0000-0001-8180-2061

Funding

Newborn Neurons in the Adult Hippocampal NetworkR01NS064025 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OVERSTREET-WADICHE, LINDA · 2009 to 2023
$5.6M
Timing of Neurotransmitter ReleaseR01NS065920 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WADICHE, JACQUES · 2009 to 2018
$3.2M
AMPAR Function in Synaptic and Extrasynaptic MembranesR01NS113948 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WADICHE, JACQUES · 2019 to 2023
$2.1M
Inhibitory Neural Circuits in Dentate FunctionR01NS105438 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OVERSTREET-WADICHE, LINDA · 2018 to 2022
$2.1M
Newborn Neurons in the Adult Hippocampal NetworkR56NS064025 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OVERSTREET-WADICHE, LINDA · 2014 to 2014
$460k
NINDS NIH HHS NS064025NINDS NIH HHS NS065920NINDS NIH HHS NS105438NINDS NIH HHS R01 NS064025NINDS NIH HHS R01 NS065920NINDS NIH HHS R01 NS105438NINDS NIH HHS R01 NS113948NINDS NIH HHS R56 NS064025
6 · The paper itself

Abstract

The number of neurotransmitter-filled vesicles released into the synaptic cleft with each action potential dictates the reliability of synaptic transmission. Variability of this fundamental property provides diversity of synaptic function across brain regions, but the source of this variability is unclear. The prevailing view is that release of a single (univesicular release, UVR) or multiple vesicles (multivesicular release, MVR) reflects variability in vesicle release probability, a notion that is well-supported by the calcium-dependence of release mode. However, using mouse brain slices, we now demonstrate that the number of vesicles released is regulated by the size of the readily-releasable pool, upstream of vesicle release probability. Our results point to a model wherein protein kinase A and its vesicle-associated target, synapsin, dynamically control release site occupancy to dictate the number of vesicles released without altering release probability. Together these findings define molecular mechanisms that control MVR and functional diversity of synaptic signaling.

Indexed as

Synaptic TransmissionAnimalsCalciumCalcium SignalingCyclic AMP-Dependent Protein KinasesMiceModels, BiologicalSynapsinsSynaptic VesiclesCalciumCyclic AMP-Dependent Protein KinasesSynapsinscerebellummouseneuroscienceRRPsynaptic transmissionvesicle release

Identifiers

PMID31364987
PMCPMC6716946

What OpenQuestion holds

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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.