Evidence map›Paper›PMID 29928766›Full record

ArticleThe Journal of physiology2018

Apparent calcium dependence of vesicle recruitment.

Andreas Ritzau-Jost, Lukasz Jablonski, Julio Viotti, Noa Lipstein, Jens Eilers, Stefan Hallermann

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  7. Fully-primed slowly-recovering vesicles mediate presynaptic LTP at neocortical neurons.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Calretinin-Expressing Synapses Show Improved Synaptic Efficacy with Reduced Asynchronous Release during High-Rate Activity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  12. Three small vesicular pools in sequence govern synaptic response dynamics during action potential trains.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Munc13-1 is a CaNeuron · 2021
    Article
  14. Article
  15. Direct imaging of rapid tethering of synaptic vesicles accompanying exocytosis at a fast central synapse.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. eLife · 2020
    Article
  17. Article
  18. Developmental Increase of Neocortical Presynaptic EfficacyFrontiers in synaptic neuroscience · 2019
    Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Andreas Ritzau-JostCarl-Ludwig-Institute for Physiology, Faculty of Medicine, Leipzig University, Leipzig, Germany.ORCID 0000-0002-3922-949X
Lukasz JablonskiCarl-Ludwig-Institute for Physiology, Faculty of Medicine, Leipzig University, Leipzig, Germany.ORCID 0000-0002-4288-6917
Julio ViottiCarl-Ludwig-Institute for Physiology, Faculty of Medicine, Leipzig University, Leipzig, Germany.ORCID 0000-0003-3631-6456
Noa LipsteinMax Planck Institute of Experimental Medicine, Göttingen, Germany.ORCID 0000-0002-0755-5899
Jens EilersCarl-Ludwig-Institute for Physiology, Faculty of Medicine, Leipzig University, Leipzig, Germany.ORCID 0000-0003-0497-5625
Stefan HallermannCarl-Ludwig-Institute for Physiology, Faculty of Medicine, Leipzig University, Leipzig, Germany.ORCID 0000-0001-9376-7048
Leipzig University · DEMax Planck Institute of Experimental Medicine · DEUniversitätsmedizin Göttingen · DE

Funding

German Research Foundation HA 6386/2-1German Research Foundation HA 6386/3-1
6 · The paper itself

Abstract

key pointsSynaptic transmission relies on the recruitment of neurotransmitter-filled vesicles to presynaptic release sites. Increased intracellular calcium buffering slows the recovery from synaptic depression, suggesting that vesicle recruitment is a calcium-dependent process. However, the molecular mechanisms of vesicle recruitment have only been investigated at some synapses. We investigate the role of calcium in vesicle recruitment at the cerebellar mossy fibre to granule cell synapse. We find that increased intracellular calcium buffering slows the recovery from depression following physiological stimulation. However, the recovery is largely resistant to perturbation of the molecular pathways previously shown to mediate calcium-dependent vesicle recruitment. Furthermore, we find two pools of vesicles with different recruitment speeds and show that models incorporating two pools of vesicles with different calcium-independent recruitment rates can explain our data. In this framework, increased calcium buffering prevents the release of intrinsically fast-recruited vesicles but does not change the vesicle recruitment rates themselves. ABSTRACT: During sustained synaptic transmission, recruitment of new transmitter-filled vesicles to the release site counteracts vesicle depletion and thus synaptic depression. An elevated intracellular Ca

Indexed as

Action PotentialsSynaptic TransmissionAnimalsCalciumCalmodulinCerebellar CortexExcitatory Postsynaptic PotentialsFemaleMaleMiceMice, Inbred C57BLNerve FibersPresynaptic TerminalsSynapsesSynaptic VesiclesCalciumCalmodulincalcium bufferingshort-term plasticitySynapsevesicle recruitment

Identifiers

PMID29928766
PMCPMC6166083
OpenAlexW2889724733

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.