Evidence map›Paper›PMID 19004011›Full record

ArticleHippocampus2009

AMPA receptor trafficking and synaptic plasticity require SQSTM1/p62.

Jianxiong Jiang, Kodeeswaran Parameshwaran, M Lamar Seibenhener, Myoung-Goo Kang, Vishnu Suppiramaniam, Richard L Huganir, Maria T Diaz-Meco, Marie W Wooten

Open access · greenAbstract read
In one paragraph

Article in Hippocampus, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
0.4field-weighted citation impact, top 46% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. The Roles of SQSTM1/p62 in Selective Autophagy and Oncogenic Signaling.International journal of molecular sciences · 2026
    Review
  4. Review
  5. Article
  6. GluA1 Degradation by Autophagy Contributes to Circadian Rhythm Effects on Cerebral Ischemia Injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  7. Review
  8. Review
  9. Reversing Cocaine-Induced Plasticity with Zeta Inhibitory Peptide.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  10. Autophagic Regulation of p62 is Critical for Cancer Therapy.International journal of molecular sciences · 2018
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. PKMζ, but not PKCλ, is rapidly synthesized and degraded at the neuronal synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  17. Article
  18. Review
  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

8 authors at 3 institutions in 1 country.

Jianxiong JiangDepartment of Biological Sciences and Program in Cellular and Molecular Biosciences, Auburn University, Auburn, Alabama 36849, USA.
Kodeeswaran Parameshwaran
M Lamar Seibenhener
Myoung-Goo Kang
Vishnu Suppiramaniam
Richard L Huganir
Maria T Diaz-Meco
Marie W Wooten
Auburn University · USJohns Hopkins University · USUniversity of Cincinnati · US

Funding

PDZ DOMAINS AND EXCITATORY SYNAPTIC FUNCTIONR01NS036715 · NINDS · JOHNS HOPKINS UNIVERSITY · PI HUGANIR, RICHARD L · 1997 to 2020
$8.6M
NERVE GROWTH FACTOR SIGNALLINGR01NS033661 · NINDS · AUBURN UNIVERSITY AT AUBURN · PI WOOTEN, MICHAEL C · 1995 to 2013
$2.7M
Howard Hughes Medical InstituteNINDS NIH HHS NS33661NINDS NIH HHS R01 NS033661NINDS NIH HHS R01 NS036715
6 · The paper itself

Abstract

SQSTM1/p62 is a multidomain/scaffold for the atypical protein kinase Cs (aPKC). Phosphorylation of AMPA receptors by PKC has been shown to regulate their insertion in the postsynaptic membrane. Here, we directly tested whether p62 could interact with AMPA receptor subunits and influence their trafficking and phosphorylation. GluR1 receptor intracellular loop L2-3 and the ZZ-type zinc finger domain of p62 are essential for the interaction between these two proteins. In this context, both p62 and aPKC-mediated phosphorylation were necessary for surface delivery of the receptor. Our findings reveal that p62 is the first protein identified that interacts with a region of the GluR receptor other than the C-terminal tail. Furthermore, mice deficient in p62 displayed impaired hippocampal CA1 long-term potentiation (LTP), along with diminished surface expression of GluR1 and phosphorylation of S818. Lastly, we identify a conserved sequence (ISExSL) shared by all p62 interacting-aPKC substrates. These findings support a model where p62 interaction and aPKC phosphorylation act together to mediate AMPA receptor trafficking and long-term synaptic plasticity in the hippocampus.

Indexed as

Synaptic TransmissionAdaptor Proteins, Signal TransducingAmino Acid SequenceAnimalsBinding SitesCell LineCell MembraneConserved SequenceHeat-Shock ProteinsHippocampusHumansMembrane PotentialsMiceMice, KnockoutMolecular Sequence DataNeuronal PlasticityAdaptor Proteins, Signal TransducingHeat-Shock ProteinsPKC-3 proteinProtein Kinase CReceptors, AMPASequestosome-1 ProteinSqstm1 protein, mouse

Identifiers

PMID19004011
PMCPMC2745981
OpenAlexW2168971983

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.