Evidence map›Paper›PMID 24274737›Full record

ReviewAnnual review of physiology2014

Molecular mechanisms for synchronous, asynchronous, and spontaneous neurotransmitter release.

Pascal S Kaeser, Wade G Regehr

Abstract readReview
In one paragraph

Review in Annual review of physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 281 papers.

0numbers the graph read from it
0cells of the map it votes in
281citing 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

281 citing papers in PubMed.

  1. Article
  2. Article
  3. The Synaptic Vesicle Priming Protein Munc13 Mediates Evoked Somatodendritic Dopamine Release.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  4. Article
  5. Review
  6. Nociceptor-enriched CAPS1 isoform couples to CabioRxiv : the preprint server for biology · 2026
    Article
  7. Presynaptic CabioRxiv : the preprint server for biology · 2026
    Article
  8. Munc13 serves as a molecular filter for SNARE sorting and assembly in active zone condensates.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Munc13-1 couples DAG and CaScience advances · 2026
    Article
  14. Article
  15. Molecular Physiology of the Neuronal Synapse.Current issues in molecular biology · 2026
    Review
  16. Review
  17. Article
  18. Membrane Merger Dynamics in Exocytosis and Endocytosis.Advances in experimental medicine and biology · 2026
    Review
  19. Review
  20. Review

221 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.

Pascal S KaeserDepartment of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115; email: kaeser@hms.harvard.edu , wade_regehr@hms.harvard.edu.
Wade G Regehr

Funding

Short-Term Synaptic Plasticity in the CNSR01NS032405 · NINDS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI REGEHR, WADE G · 1995 to 2016
$4.8M
Function of RIM-dependent Synaptic Plasticity in Cocaine-induced BehaviorsK01DA029044 · NIDA · STANFORD UNIVERSITY · PI KAESER, PASCAL SIMON · 2010 to 2014
$720k
NIDA NIH HHS K01 DA029044NINDS NIH HHS R01 NS032405NINDS NIH HHS R01 NS32405
6 · The paper itself

Abstract

Most neuronal communication relies upon the synchronous release of neurotransmitters, which occurs through synaptic vesicle exocytosis triggered by action potential invasion of a presynaptic bouton. However, neurotransmitters are also released asynchronously with a longer, variable delay following an action potential or spontaneously in the absence of action potentials. A compelling body of research has identified roles and mechanisms for synchronous release, but asynchronous release and spontaneous release are less well understood. In this review, we analyze how the mechanisms of the three release modes overlap and what molecular pathways underlie asynchronous and spontaneous release. We conclude that the modes of release have key fusion processes in common but may differ in the source of and necessity for Ca(2+) to trigger release and in the identity of the Ca(2+) sensor for release.

Indexed as

AnimalsCalciumExocytosisHumansNeurotransmitter AgentsReceptors, PresynapticSNARE ProteinsSynaptic TransmissionSynaptic VesiclesCalciumNeurotransmitter AgentsReceptors, PresynapticSNARE Proteins

Identifiers

PMID24274737
PMCPMC4503208

What OpenQuestion holds

Textmetadata
LicenceTDM
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.