Evidence map›Paper›PMID 38853547›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2024

Synapse-specific structural plasticity that protects and refines local circuits during LTP and LTD.

Kristen M Harris, Masaaki Kuwajima, Juan C Flores, Karen Zito

Abstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Molecular Physiology of the Neuronal Synapse.Current issues in molecular biology · 2026
    Review
  5. Review
  6. Review
  7. Review
  8. Role and mechanisms of interneurons in chronic pain and pain-induced cognitive impairment.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Review
  9. Long-term potentiation: 50 years on: past, present and future.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    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

4 authors.

Kristen M HarrisDepartment of Neuroscience and Center for Learning and Memory, The University of Texas at Austin , Austin, TX 78712, USA.ORCID 0000-0002-1943-4744
Masaaki KuwajimaDepartment of Neuroscience and Center for Learning and Memory, The University of Texas at Austin , Austin, TX 78712, USA.ORCID 0000-0002-1478-3726
Juan C FloresCenter for Neuroscience, University of California , Davis, CA 95618, USA.ORCID 0000-0003-3957-8670
Karen ZitoCenter for Neuroscience, University of California , Davis, CA 95618, USA.ORCID 0000-0002-0799-0460

Funding

Synaptic plasticity across the lifespanR01MH095980 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI KRISTEN M HARRIS · 2012 to 2026
$5.0M
Mechanisms of Dendritic Spine EliminationR01NS062736 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ZITO, KAREN · 2009 to 2019
$3.8M
Division of Biological InfrastructureNational Institute of Neurological Disorders & Stroke R01NS06736NIMH NIH HHS R01 MH095980NINDS NIH HHS R01 NS062736
6 · The paper itself

Abstract

Synapses form trillions of connections in the brain. Long-term potentiation (LTP) and long-term depression (LTD) are cellular mechanisms vital for learning that modify the strength and structure of synapses. Three-dimensional reconstruction from serial section electron microscopy reveals three distinct pre- to post-synaptic arrangements: strong active zones (AZs) with tightly docked vesicles, weak AZs with loose or non-docked vesicles, and nascent zones (NZs) with a postsynaptic density but no presynaptic vesicles. Importantly, LTP can be temporarily saturated preventing further increases in synaptic strength. At the onset of LTP, vesicles are recruited to NZs, converting them to AZs. During recovery of LTP from saturation (1-4 h), new NZs form, especially on spines where AZs are most enlarged by LTP. Sentinel spines contain smooth endoplasmic reticulum (SER), have the largest synapses and form clusters with smaller spines lacking SER after LTP recovers. We propose a model whereby NZ plasticity provides synapse-specific AZ expansion during LTP and loss of weak AZs that drive synapse shrinkage during LTD. Spine clusters become functionally engaged during LTP or disassembled during LTD. Saturation of LTP or LTD probably acts to protect recently formed memories from ongoing plasticity and may account for the advantage of spaced over massed learning. This article is part of a discussion meeting issue 'Long-term potentiation: 50 years on'.

Indexed as

Long-Term PotentiationLong-Term Synaptic DepressionNeuronal PlasticitySynapsesAnimalsDendritic SpinesModels, Neurologicallong-term depressionlong-term potentiationspaced learningsynapseultrastructure

Identifiers

PMID38853547
PMCPMC11529630

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.