Evidence map›Paper›PMID 26858418›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Variable priming of a docked synaptic vesicle.

Jae Hoon Jung, Joseph A Szule, Robert M Marshall, Uel J McMahan

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Article
  2. 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
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. The Mechanical Basis of Memory - the MeshCODE Theory.Frontiers in molecular neuroscience · 2021
    Article
  14. Article
  15. Continuum Models of Membrane Fusion: Evolution of the Theory.International journal of molecular sciences · 2020
    Review
  16. Review
  17. Nanomachinery Organizing Release at Neuronal and Ribbon Synapses.International journal of molecular sciences · 2019
    Review
  18. Differentiation and Characterization of Excitatory and Inhibitory Synapses by Cryo-electron Tomography and Correlative Microscopy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  19. 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

4 authors.

Jae Hoon JungDepartment of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305; Department of Physics, Stanford University School of Humanities and Sciences, Stanford, CA 94305; Department of Biology, Texas A&M University, College Station, TX 77845.
Joseph A SzuleDepartment of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305; Department of Biology, Texas A&M University, College Station, TX 77845.
Robert M MarshallDepartment of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305; Department of Biology, Texas A&M University, College Station, TX 77845.
Uel J McMahanDepartment of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305; Department of Biology, Texas A&M University, College Station, TX 77845 grantser@tamu.edu.

Funding

Structure of the Active Zone at Nanometer ScaleR01NS014506 · NINDS · STANFORD UNIVERSITY · PI MCMAHAN, UEL J · 1985 to 2006
$3.4M
Improvement and Extension of EM3DR01MH068065 · NIMH · STANFORD UNIVERSITY · PI MCMAHAN, UEL J · 2003 to 2007
$2.5M
NERVOUS SYSTEM REGENERATION AND PLASTICITYT32NS007158 · NINDS · STANFORD UNIVERSITY · PI KNUDSEN, ERIC · 1985 to 2004
$461k
NIMH NIH HHS MH068065NIMH NIH HHS R01 MH068065NINDS NIH HHS NS007158NINDS NIH HHS NS014506NINDS NIH HHS R01 NS014506NINDS NIH HHS T32 NS007158
6 · The paper itself

Abstract

The priming of a docked synaptic vesicle determines the probability of its membrane (VM) fusing with the presynaptic membrane (PM) when a nerve impulse arrives. To gain insight into the nature of priming, we searched by electron tomography for structural relationships correlated with fusion probability at active zones of axon terminals at frog neuromuscular junctions. For terminals fixed at rest, the contact area between the VM of docked vesicles and PM varied >10-fold with a normal distribution. There was no merging of the membranes. For terminals fixed during repetitive evoked synaptic transmission, the normal distribution of contact areas was shifted to the left, due in part to a decreased number of large contact areas, and there was a subpopulation of large contact areas where the membranes were hemifused, an intermediate preceding complete fusion. Thus, fusion probability of a docked vesicle is related to the extent of its VM-PM contact area. For terminals fixed 1 h after activity, the distribution of contact areas recovered to that at rest, indicating the extent of a VM-PM contact area is dynamic and in equilibrium. The extent of VM-PM contact areas in resting terminals correlated with eccentricity in vesicle shape caused by force toward the PM and with shortness of active zone material macromolecules linking vesicles to PM components, some thought to include Ca(2+) channels. We propose that priming is a variable continuum of events imposing variable fusion probability on each vesicle and is regulated by force-generating shortening of active zone material macromolecules in dynamic equilibrium.

Indexed as

Electron Microscope TomographySynaptic MembranesSynaptic VesiclesAnimalsCalcium ChannelsRana pipiensCalcium Channelsactive zone materialelectron tomographyhemifusionprimingsynapse

Identifiers

PMID26858418
PMCPMC4776491

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.