Evidence map›Paper›PMID 21347244›Full record

ArticlePloS one2011

ApoE receptor 2 regulates synapse and dendritic spine formation.

Sonya B Dumanis, Hyun-Jung Cha, Jung Min Song, Justin H Trotter, Matthew Spitzer, Ji-Yun Lee, Edwin J Weeber, R Scott Turner, Daniel T S Pak, G William Rebeck and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

32 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. The apolipoprotein receptor LRP3 compromises APP levels.Alzheimer's research & therapy · 2021
    Article
  9. Review
  10. ApoER2: Functional Tuning Through Splicing.Frontiers in molecular neuroscience · 2020
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Role of BACE1 in Alzheimer's synaptic function.Translational neurodegeneration · 2017
    Review
  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

11 authors at 3 institutions in 1 country.

Sonya B DumanisDepartment of Neuroscience, Georgetown University Medical Center, Washington, DC, United States of America.
Hyun-Jung Cha
Jung Min Song
Justin H Trotter
Matthew Spitzer
Ji-Yun Lee
Edwin J Weeber
R Scott Turner
Daniel T S Pak
G William Rebeck
Hyang-Sook Hoe
Georgetown University · USGeorgetown University Medical Center · USUniversity of South Florida · US

Funding

TRANSGENIC MOUSE COREP01AG030128 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BU, GUOJUN · 2009 to 2013
$9.4M
Mechanism of Abeta SequestrationR01AG026478 · NIA · GEORGETOWN UNIVERSITY · PI TURNER, RAYMOND SCOTT · 2007 to 2011
$1.4M
Molecular mechanisms of synapse lossR01NS048085 · NINDS · GEORGETOWN UNIVERSITY · PI PAK, DANIEL T · 2006 to 2010
$1.4M
ApoE and ApoE receptors in the molecular mechanisms of synapse formationR03AG032330 · NIA · GEORGETOWN UNIVERSITY · PI HOE, HYANG-SOOK · 2008 to 2009
$207k
APP in neuronal development through extracellular matrix interactionsR03AG034253 · NIA · GEORGETOWN UNIVERSITY · PI HOE, HYANG-SOOK · 2010 to 2011
$132k
NIA NIH HHS AG026478NIA NIH HHS AG032330NIA NIH HHS AG032330-02S1NIA NIH HHS AG034253NIA NIH HHS P01 AG030128NIA NIH HHS R01 AG026478NIA NIH HHS R03 AG032330NIA NIH HHS R03 AG034253NINDS NIH HHS NS048085NINDS NIH HHS R01 NS048085
6 · The paper itself

Abstract

backgroundApolipoprotein E receptor 2 (ApoEr2) is a postsynaptic protein involved in long-term potentiation (LTP), learning, and memory through unknown mechanisms. We examined the biological effects of ApoEr2 on synapse and dendritic spine formation-processes critical for learning and memory. METHODOLOGY/PRINCIPAL

findingsIn a heterologous co-culture synapse assay, overexpression of ApoEr2 in COS7 cells significantly increased colocalization with synaptophysin in primary hippocampal neurons, suggesting that ApoEr2 promotes interaction with presynaptic structures. In primary neuronal cultures, overexpression of ApoEr2 increased dendritic spine density. Consistent with our in vitro findings, ApoEr2 knockout mice had decreased dendritic spine density in cortical layers II/III at 1 month of age. We also tested whether the interaction between ApoEr2 and its cytoplasmic adaptor proteins, specifically X11α and PSD-95, affected synapse and dendritic spine formation. X11α decreased cell surface levels of ApoEr2 along with synapse and dendritic spine density. In contrast, PSD-95 increased cell surface levels of ApoEr2 as well as synapse and dendritic spine density. CONCLUSIONS/SIGNIFICANCE: These results suggest that ApoEr2 plays important roles in structure and function of CNS synapses and dendritic spines, and that these roles are modulated by cytoplasmic adaptor proteins X11α and PSD-95.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsChlorocebus aethiopsCoculture TechniquesCOS CellsCytoplasmDendritic SpinesDisks Large Homolog 4 ProteinExtracellular SpaceGuanylate KinasesHippocampusHumansLDL-Receptor Related ProteinsMembrane ProteinsMiceNerve Tissue ProteinsAdaptor Proteins, Signal TransducingApba1 protein, mouseDisks Large Homolog 4 ProteinDlg4 protein, mouseGuanylate KinasesLDL-Receptor Related Proteinslow density lipoprotein receptor-related protein 8Membrane ProteinsNerve Tissue ProteinsReceptors, AMPA

Identifiers

PMID21347244
PMCPMC3039666
OpenAlexW2045877537

What OpenQuestion holds

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LicenceCC BY
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.