Evidence map›Paper›PMID 33875591›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Shortened tethering filaments stabilize presynaptic vesicles in support of elevated release probability during LTP in rat hippocampus.

Jae Hoon Jung, Lyndsey M Kirk, Jennifer N Bourne, Kristen M Harris

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Presynaptic Vesicles Supply Membrane for Axonal Bouton Enlargement during Long Term Potentiation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Equal levels of pre- and postsynaptic potentiation produce unequal outcomes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  10. Synapse-specific structural plasticity that protects and refines local circuits during LTP and LTD.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  11. Frequency of Spontaneous Neurotransmission at Individual Boutons Corresponds to the Size of the Readily Releasable Pool of Vesicles.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  12. Article
  13. 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
  14. Modification of the synaptic cleft under excitatory conditions.Frontiers in synaptic neuroscience · 2023
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. A sequential two-step priming scheme reproduces diversity in synaptic strength and short-term plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  20. 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

4 authors at 3 institutions in 1 country.

Jae Hoon JungLaboratory of Neurobiology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0002-2187-2495
Lyndsey M KirkDepartment of Neuroscience, Center for Learning and Memory, Institute for Neuroscience, University of Texas at Austin, Austin, TX 78712.ORCID 0000-0002-5125-652X
Jennifer N BourneDepartment of Neuroscience, Center for Learning and Memory, Institute for Neuroscience, University of Texas at Austin, Austin, TX 78712.
Kristen M HarrisDepartment of Neuroscience, Center for Learning and Memory, Institute for Neuroscience, University of Texas at Austin, Austin, TX 78712; kharris@utexas.edu.ORCID 0000-0002-1943-4744
The University of Texas at Austin · USNational Institutes of Health · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Synaptic plasticity across the lifespanR01MH095980 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI KRISTEN M HARRIS · 2012 to 2026
$5.0M
Spine and Synaptic Plasticity in Mature HippocampusR37NS021184 · NINDS · UNIVERSITY OF TEXAS AT AUSTIN · PI HARRIS, KRISTEN M · 2005 to 2011
$2.2M
Synapse growth and elimination in mature CNSR01MH104319 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI HARRIS, KRISTEN M · 2014 to 2018
$1.8M
Distance-Dependent Structure and Function of Neuronal DendritesR01NS074644 · NINDS · UNIVERSITY OF TEXAS AT AUSTIN · PI HARRIS, KRISTEN M · 2011 to 2015
$1.7M
ONTOGENY OF STRUCTURE &FUNCTION AT HIPPOCAMPAL SYNAPSESR01NS033574 · NINDS · UNIVERSITY OF TEXAS AUSTIN · PI HARRIS, KRISTEN M · 1996 to 2005
$1.5M
SPINES SYNAPSES AND THE ONTOGENY OF A MEMORY MECHANISMR01NS021184 · NINDS · MEDICAL COLLEGE OF GEORGIA (MCG) · PI HARRIS, KRISTEN M · 1988 to 2003
$1.4M
Synaptic plasticity across the lifespanR56MH095980 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI HARRIS, KRISTEN M · 2019 to 2019
$619k
Mapping the macromolecular architecture of the synaptic basal lamina at neuromuscular junctions and localizing the C-terminus of neural agrin in itR21NS102788 · NINDS · TEXAS A&M UNIVERSITY · PI MCMAHAN, UEL J · 2017 to 2018
$408k
NIMH NIH HHS R01 MH095980NIMH NIH HHS R01 MH104319NIMH NIH HHS R56 MH095980NINDS NIH HHS R01 NS021184NINDS NIH HHS R01 NS033574NINDS NIH HHS R01 NS074644NINDS NIH HHS R21 NS102788NINDS NIH HHS R37 NS021184
6 · The paper itself

Abstract

Long-term potentiation (LTP) is a cellular mechanism of learning and memory that results in a sustained increase in the probability of vesicular release of neurotransmitter. However, previous work in hippocampal area CA1 of the adult rat revealed that the total number of vesicles per synapse decreases following LTP, seemingly inconsistent with the elevated release probability. Here, electron-microscopic tomography (EMT) was used to assess whether changes in vesicle density or structure of vesicle tethering filaments at the active zone might explain the enhanced release probability following LTP. The spatial relationship of vesicles to the active zone varies with functional status. Tightly docked vesicles contact the presynaptic membrane, have partially formed SNARE complexes, and are primed for release of neurotransmitter upon the next action potential. Loosely docked vesicles are located within 8 nm of the presynaptic membrane where SNARE complexes begin to form. Nondocked vesicles comprise recycling and reserve pools. Vesicles are tethered to the active zone via filaments composed of molecules engaged in docking and release processes. The density of tightly docked vesicles was increased 2 h following LTP compared to control stimulation, whereas the densities of loosely docked or nondocked vesicles congregating within 45 nm above the active zones were unchanged. The tethering filaments on all vesicles were shorter and their attachment sites shifted closer to the active zone. These findings suggest that tethering filaments stabilize more vesicles in the primed state. Such changes would facilitate the long-lasting increase in release probability following LTP.

Indexed as

AnimalsBrainCytoskeletonElectron Microscope TomographyHippocampusLong-Term PotentiationMaleNeurotransmitter AgentsPresynaptic TerminalsRatsRats, Long-EvansSynapsesSynaptic MembranesSynaptic VesiclesNeurotransmitter Agentslong-term potentiationnanoscalesynaptic plasticityultrastructure

Identifiers

PMID33875591
PMCPMC8092591
OpenAlexW3152526524

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.