Evidence map›Paper›PMID 12684438›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2003

Imaging calcium entry sites and ribbon structures in two presynaptic cells.

David Zenisek, Viviana Davila, Lei Wan, Wolfhard Almers

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing 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

103 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Role of Ribeye PXDLS/T-binding cleft in normal synaptic ribbon function.bioRxiv : the preprint server for biology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Transmission at rod and cone ribbon synapses in the retina.Pflugers Archiv : European journal of physiology · 2021
    Review
  11. Review
  12. Article
  13. Rapid CaProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. Phase-Locking Requires Efficient CaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  15. Article
  16. Article
  17. Dynamic L-type CaBiochimica et biophysica acta. Molecular cell research · 2018
    Article
  18. Review
  19. CaFrontiers in cellular neuroscience · 2018
    Article
  20. Article

43 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

4 authors.

David ZenisekDepartment of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Viviana Davila
Lei Wan
Wolfhard Almers

Funding

TRANSCRIPTIONAL REGULATION BY THE CAM CASCADEP01DK044239 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI GOODMAN, RICHARD H. · 1992 to 2006
$9.6M
MULTIDISCIPLINARY TRAINING IN NEUROENDOCRINOLOGYT32DK007680 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI GOODMAN, RICHARD H. · 1991 to 2015
$6.8M
SINGLE EXO/ENDOCYTIC EVENTS IN NEURONS &ENDOCRINE CELLSR01MH060600 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI ALMERS, WOLFHARD · 2000 to 2015
$6.2M
NIDDK NIH HHS DK07680NIDDK NIH HHS DK44239NIDDK NIH HHS P01 DK044239NIDDK NIH HHS T32 DK007680NIMH NIH HHS MH60600NIMH NIH HHS R01 MH060600
6 · The paper itself

Abstract

We investigated the location of calcium entry sites and synaptic ribbons in the type-Mb goldfish bipolar neuron and the bullfrog saccular hair cell. Cells were loaded with a fast calcium indicator (Fluo-3 or Fluo-5F) and an excess of a high-affinity but slow Ca buffer (EGTA). The cell surface was imaged by evanescent field microscopy. Small fluorescent "hot spots" representing calcium entry sites appeared abruptly when a voltage step opened Ca channels and disappeared or dimmed abruptly when Ca channels closed. In bipolar cells, the fluorescence of hot spots tracked the calcium influx. Hair cells showed similar Ca hot spots. Synaptic ribbons or dense bodies were labeled by immunofluorescence with an antibody that recognizes the ribbon protein ribeye. The antibody labeled punctate structures beneath the plasma membrane. In both bipolar neurons and hair cells, the number of Ca entry sites was similar or identical to that of ribbons or dense bodies, consistent with the idea that calcium-channel clusters reside near ribbons, and that both mark active zones. In bipolar cells, the number of Ca entry sites and ribeye-positive fluorescent spots is also strikingly similar to that of exocytic active zones but significantly less than the number of total exocytic sites including solitary fusion events outside active zones. We suggest that in bipolar terminals, active zones, Ca entry sites, and synaptic ribbons all colocalize, but also that a significant number of vesicles can fuse outside active zones and, hence, independently of synaptic ribbons.

Indexed as

Alcohol OxidoreductasesAnimalsCalciumCalcium ChannelsCells, CulturedCulture TechniquesDNA-Binding ProteinsElectric ConductivityExocytosisEye ProteinsFluorescenceGoldfishHair Cells, AuditoryIon TransportMembrane FusionMicroscopy, FluorescenceAlcohol OxidoreductasesCalciumCalcium ChannelsC-terminal binding proteinDNA-Binding ProteinsEye ProteinsPhosphoproteins

Identifiers

PMID12684438
PMCPMC6742070

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.