Evidence map›Paper›PMID 30600260›Full record

ReviewScience signaling2019

Mechanisms of postsynaptic localization of AMPA-type glutamate receptors and their regulation during long-term potentiation.

Olivia R Buonarati, Erik A Hammes, Jake F Watson, Ingo H Greger, Johannes W Hell

Open access · greenAbstract readReview
In one paragraph

Review in Science signaling, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 83 citations in OpenAlex.

  1. 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
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Synthesis of [Molecules (Basel, Switzerland) · 2024
    Article
  13. Article
  14. Article
  15. Plasma metabonomic study on the effect ofMolecular medicine reports · 2023
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

5 authors at 2 institutions in 2 countries.

Olivia R BuonaratiDepartment of Pharmacology, University of California at Davis, Davis, CA 95616-8636, USA.ORCID 0000-0001-6530-6797
Erik A HammesDepartment of Pharmacology, University of California at Davis, Davis, CA 95616-8636, USA.ORCID 0000-0003-2327-7101
Jake F WatsonNeurobiology Division, MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.ORCID 0000-0002-8698-3823
Ingo H GregerNeurobiology Division, MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.ORCID 0000-0002-7291-2581
Johannes W HellDepartment of Pharmacology, University of California at Davis, Davis, CA 95616-8636, USA. jwhell@ucdavis.edu.ORCID 0000-0001-7960-7531
University of California, Davis · USMRC Laboratory of Molecular Biology · GB

Funding

Role of a-actinin in Cav1.2 FunctionR01AG055357 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI JOHANNES W HELL · 2016 to 2026
$4.0M
Molecular Mechanisms of Postsynaptic AMPA Receptor LocalizationR01MH097887 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2014 to 2018
$2.5M
Learning, Memory, and Plasticity (LaMP) Training ProgramT32MH112507 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Karen Zito · 2017 to 2026
$2.4M
Signaling by cAMP within postsynaptic nano domains R01NS078792R01NS078792 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2012 to 2016
$2.0M
MRP4 extrudes cAMP for localized regulation of calcium channel activityF31NS086226 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ASFAHA, OLIVIA RUTH · 2013 to 2015
$110k
Biotechnology and Biological Sciences Research Council BB/N002113/1Medical Research Council MC_U105174197NIA NIH HHS R01 AG055357NIMH NIH HHS R01 MH097887NIMH NIH HHS T32 MH112507NINDS NIH HHS F31 NS086226NINDS NIH HHS R01 NS078792
6 · The paper itself

Abstract

l-Glutamate is the main excitatory neurotransmitter in the brain, with postsynaptic responses to its release predominantly mediated by AMPA-type glutamate receptors (AMPARs). A critical component of synaptic plasticity involves changes in the number of responding postsynaptic receptors, which are dynamically recruited to and anchored at postsynaptic sites. Emerging findings continue to shed new light on molecular mechanisms that mediate AMPAR postsynaptic trafficking and localization. Accordingly, unconventional secretory trafficking of AMPARs occurs in dendrites, from the endoplasmic reticulum (ER) through the ER-Golgi intermediary compartment directly to recycling endosomes, independent of the Golgi apparatus. Upon exocytosis, AMPARs diffuse in the plasma membrane to reach the postsynaptic site, where they are trapped to contribute to transmission. This trapping occurs through a combination of both intracellular interactions, such as TARP (transmembrane AMPAR regulatory protein) binding to α-actinin-stabilized PSD-95, and extracellular interactions through the receptor amino-terminal domain. These anchoring mechanisms may facilitate precise receptor positioning with respect to glutamate release sites to enable efficient synaptic transmission.

Indexed as

AnimalsDendritesHumansLong-Term PotentiationProtein TransportReceptors, AMPAReceptors, GlutamateSynapsesSynaptic PotentialsSynaptic TransmissionReceptors, AMPAReceptors, Glutamate

Identifiers

PMID30600260
PMCPMC7175813
OpenAlexW2906908462

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.