Evidence map›Paper›PMID 12428806›Full record

ReviewNeuromolecular medicine2002

Synaptic vesicle endocytosis: the races, places, and molecular faces.

Jennifer R Morgan, George J Augustine, Eileen M Lafer

Abstract readReview
PubMed Publisher
In one paragraph

Review in Neuromolecular medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Dysfunction of Synaptic Vesicle Endocytosis in Parkinson's Disease.Frontiers in integrative neuroscience · 2021
    Review
  3. Article
  4. Review
  5. Article
  6. A role for an Hsp70 nucleotide exchange factor in the regulation of synaptic vesicle endocytosis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  7. Article
  8. Article
  9. Role of HRB in clathrin-dependent endocytosis.The Journal of biological chemistry · 2008
    Article
  10. UNC-13 and UNC-10/rim localize synaptic vesicles to specific membrane domains.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
    Article
  11. Review
  12. Article
  13. A role for talin in presynaptic function.The Journal of cell biology · 2004
    Article
  14. Article
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.

Jennifer R MorganYale University School of Medicine--HHMI, Department of Cell Biology, New Haven, CT 06510, USA.
George J Augustine
Eileen M Lafer

Funding

MOLECULAR BIOLOGY OF THE SYNAPSER01NS029051 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LAFER, EILEEN M. · 1990 to 2012
$4.0M
ROLE OF CALCIUM IONS IN PRESYNAPTIC FUNCTIONR01NS021624 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI AUGUSTINE, GEORGE J. · 1985 to 2009
$3.2M
Molecular Biology of the SynapseR56NS029051 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LAFER, EILEEN M. · 2008 to 2013
$744k
NINDS NIH HHS NS-21624NINDS NIH HHS NS-29051NINDS NIH HHS R01 NS029051
6 · The paper itself

Abstract

The classical experiments on synaptic vesicle recycling in the 1970s by Heuser and Reese, Ceccarelli, and their colleagues raised opposing theories regarding the speed, mechanisms, and locations of membrane retrieval at the synapse. The Heuser and Reese experiments supported a model in which synaptic vesicle recycling is mediated by the formation of coated vesicles, is relatively slow, and occurs distally from active zones, the sites of neurotransmitter release. Because heavy levels of stimulation were needed to visualize the coated vesicles, Ceccarelli's experiments argued that synaptic vesicle recycling does not require the formation of coated vesicles, is relatively fast, and occurs directly at the active zone in a "kiss-and-run" reversal of exocytosis under more physiological conditions. For the next thirty years, these models have provided the foundation for studies of the rates, locations, and molecular elements involved in synaptic vesicle endocytosis. Here, we describe the evidence supporting each model and argue that the coated vesicle pathway is the most predominant physiological mechanism for recycling synaptic vesicles.

Indexed as

AnimalsClathrinCoated VesiclesExocytosisHumansModels, NeurologicalNervous SystemPresynaptic TerminalsSynaptic MembranesSynaptic TransmissionSynaptic VesiclesClathrin

Identifiers

PMID12428806

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.