Evidence map›Paper›PMID 18495874›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2008

Evidence that vesicles undergo compound fusion on the synaptic ribbon.

Gary Matthews, Peter Sterling

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

66 citing papers in PubMed, 108 citations in OpenAlex.

  1. Membrane Merger Dynamics in Exocytosis and Endocytosis.Advances in experimental medicine and biology · 2026
    Review
  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. Review
  5. Review
  6. Three-Dimensional Ultrastructure of the Normal Rod Photoreceptor Synapse and Degenerative Changes Induced by Retinal Detachment.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. The Decade of Super-Resolution Microscopy of the Presynapse.Frontiers in synaptic neuroscience · 2020
    Review
  15. CaFrontiers in cellular neuroscience · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

6 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 1 country.

Gary MatthewsDepartment of Neurobiology and Behavior, State University of New York, Stony Brook, Stony Brook, New York 11794-5230, USA. gary.g.matthews@sunysb.edu
Peter Sterling
Stony Brook University · USUniversity of Pennsylvania · US

Funding

CELLULAR NEUROPHYSIOLOGY OF THE VERTEBRATE RETINAR01EY003821 · NEI · STATE UNIVERSITY NEW YORK STONY BROOK · PI WOLLMUTH, LONNIE P · 1985 to 2019
$8.1M
STRUCTURE AND FUNCTION OF PARALLEL CHANNELS IN THE FOVEAR01EY008124 · NEI · UNIVERSITY OF PENNSYLVANIA · PI STERLING, PETER · 1989 to 2008
$3.6M
NEI NIH HHS EY03821NEI NIH HHS EY08124NEI NIH HHS R01 EY003821NEI NIH HHS R01 EY008124
6 · The paper itself

Abstract

The ribbon synapse can release a stream of transmitter quanta at very high rates. Although the ribbon tethers numerous vesicles near the presynaptic membrane, most of the tethered vesicles are held at a considerable distance from the plasma membrane. Therefore, it remains unclear how their contents are released. We evoked prolonged bouts of exocytosis from a retinal bipolar cell, fixed within seconds, and then studied the ribbons by electron microscopy. Vesicle density on ribbons was reduced by approximately 50% compared with cells where exocytosis was blocked with intracellular ATP-gammaS. Large, irregularly shaped vesicles appeared on the ribbon in cells fixed during repetitive stimulation of exocytosis, and in some cases the large vesicles could be traced in adjacent sections to cisternae open to the medium. The large cisternal structures were attached to the ribbon by filaments similar to those that tether synaptic vesicles to the ribbon, and they occupied the base of the ribbon near the plasma membrane, where normal synaptic vesicles are found in resting cells. We suggest that the cisternae attached to ribbons represent synaptic vesicles that fused by compound exocytosis during strong repetitive stimulation and, thus, that vesicles tethered to the ribbon can empty their contents by fusing to other vesicles docked at the presynaptic membrane. Such compound fusion could explain the extremely high release rates and the multivesicular release reported for auditory and visual ribbon synapses.

Indexed as

Action PotentialsAdenosine TriphosphateAnimalsCalciumExocytosisGABA AgonistsGoldfishMembrane FusionMicroscopy, Electron, TransmissionMuscimolPatch-Clamp TechniquesPotassiumPresynaptic TerminalsRetinaRetinal Bipolar CellsSynaptic Vesiclesadenosine 5'-O-(3-thiotriphosphate)Adenosine TriphosphateCalciumGABA AgonistsMuscimolPotassium

Identifiers

PMID18495874
PMCPMC2409142
OpenAlexW2070338208

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.