Evidence map›Paper›PMID 17242349›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Imaging synaptosomal calcium concentration microdomains and vesicle fusion by using total internal reflection fluorescent microscopy.

Yafell Serulle, Mutsuyuki Sugimori, Rodolfo R Llinás

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 35 citations in OpenAlex.

  1. ZIP-ZnT1 complexes mediate a local ZnCellular and molecular life sciences : CMLS · 2026
    Article
  2. Review
  3. Article
  4. The interplay between mitochondria and store-operated CaJournal of cellular and molecular medicine · 2021
    Review
  5. Article
  6. Article
  7. Reduced endogenous Ca2+ buffering speeds active zone Ca2+ signaling.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  8. Absolute position total internal reflection microscopy with an optical tweezer.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  9. Article
  10. Properties of ribbon and non-ribbon release from rod photoreceptors revealed by visualizing individual synaptic vesicles.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. The Na-K-ATPase and calcium-signaling microdomains.Physiology (Bethesda, Md.) · 2008
    Review
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

3 authors at 2 institutions in 1 country.

Yafell SerulleProgram in Neuroscience and Physiology, Department of Biochemistry, New York University School of Medicine, New York, NY 10016, USA.
Mutsuyuki Sugimori
Rodolfo R Llinás
Marine Biological Laboratory · USNew York University · US

Funding

VISUAL-VESTIBULAR INTERACTION IN EYE MOVEMENT CONTROLP01NS013742 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LLINAS, RODOLFO R · 1985 to 2011
$15.6M
NINDS NIH HHS NS13742NINDS NIH HHS P01 NS013742
6 · The paper itself

Abstract

Transmitter release at chemical synapses is triggered by high calcium concentration microprofiles at the presynaptic cytosol. Such microprofiles, generated by the opening of voltage-dependent calcium channels at the presynaptic plasma membrane, have been defined as calcium concentration microdomains. Using total internal reflection fluorescent microscopy in conjunction with calcium and vesicular release indicator dyes, we have directly visualized the close apposition of calcium concentration microdomains and synaptic release sites at single synaptic terminals from the CNS from rat cerebellar mossy fiber and squid optic lobe. These findings demonstrate the close apposition of calcium entry and release sites and the dynamics of such site locations over time. Kinetic analysis shows that vesicles can be released via two distinct mechanisms: full-fusion and kiss-and-run. Calcium triggers vesicular motion toward the membrane, and the speed of such movement is calcium concentration-dependent. Moreover, the immediately available vesicular pool represents molecularly trapped vesicles that can be located at a larger distance from the plasma membrane than the field illuminated by total internal reflection fluorescent microscopy.

Indexed as

AnimalsBrainCalciumCerebellumDose-Response Relationship, DrugExocytosisFluorescent DyesKineticsProtein Structure, TertiaryPyridinium CompoundsQuaternary Ammonium CompoundsRatsSpectroscopy, Fourier Transform InfraredSynapsesSynaptosomesTime FactorsCalciumFluorescent DyesFM1 43Pyridinium CompoundsQuaternary Ammonium Compounds

Identifiers

PMID17242349
PMCPMC1785242
OpenAlexW2011654614

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.