Evidence map›Paper›PMID 20628354›Full record

ArticleThe EMBO journal2010

PTEN is recruited to the postsynaptic terminal for NMDA receptor-dependent long-term depression.

Sandra Jurado, Marion Benoist, Argentina Lario, Shira Knafo, Cortney N Petrok, José A Esteban

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

85 citing papers in PubMed, 144 citations in OpenAlex.

  1. PTEN Subcellular Localization Dictates Function.bioRxiv : the preprint server for biology · 2026
    Article
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  11. Article
  12. Review
  13. Article
  14. Immunity, Ion Channels and Epilepsy.International journal of molecular sciences · 2022
    Review
  15. AMPA Receptor Function in Hypothalamic Synapses.Frontiers in synaptic neuroscience · 2022
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

25 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 2 countries.

Sandra JuradoDepartment of Pharmacology, University of Michigan Medical School, Ann Arbor, MI, USA.
Marion Benoist
Argentina Lario
Shira Knafo
Cortney N Petrok
José A Esteban
Centro de Biología Molecular Severo Ochoa · ESConsejo Superior de Investigaciones Científicas · ESUniversity of Michigan–Ann Arbor · US

Funding

Transgenic Mouse and Biobank CoreP01CA095616 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DEPINHO, RONALD ANTHONY · 2003 to 2012
$20.3M
UC Davis/NIH NeuroMab FacilityU24NS050606 · NINDS · UNIVERSITY OF CALIFORNIA DAVIS · PI TRIMMER, JAMES S · 2005 to 2014
$15.6M
Role of Rab proteins in AMPA receptor synaptic targetingR01MH070417 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MARTENS, JEFFREY · 2005 to 2009
$1.5M
NCI NIH HHS P01 CA095616NIMH NIH HHS MH070417NIMH NIH HHS R01 MH070417NINDS NIH HHS U24 NS050606
6 · The paper itself

Abstract

Phosphatase and tensin homolog deleted on chromosome ten (PTEN) is an important regulator of phosphatidylinositol-(3,4,5,)-trisphosphate signalling, which controls cell growth and differentiation. However, PTEN is also highly expressed in the adult brain, in which it can be found in dendritic spines in hippocampus and other brain regions. Here, we have investigated specific functions of PTEN in the regulation of synaptic function in excitatory hippocampal synapses. We found that NMDA receptor activation triggers a PDZ-dependent association between PTEN and the synaptic scaffolding molecule PSD-95. This association is accompanied by PTEN localization at the postsynaptic density and anchoring within the spine. On the other hand, enhancement of PTEN lipid phosphatase activity is able to drive depression of AMPA receptor-mediated synaptic responses. This activity is specifically required for NMDA receptor-dependent long-term depression (LTD), but not for LTP or metabotropic glutamate receptor-dependent LTD. Therefore, these results reveal PTEN as a regulated signalling molecule at the synapse, which is recruited to the postsynaptic membrane upon NMDA receptor activation, and is required for the modulation of synaptic activity during plasticity.

Indexed as

Long-Term Synaptic DepressionAnimalsDisks Large Homolog 4 ProteinHippocampusIntracellular Signaling Peptides and ProteinsMembrane ProteinsPDZ DomainsPTEN PhosphohydrolaseRatsReceptors, AMPAReceptors, N-Methyl-D-AspartateSpineSynapsesSynaptic TransmissionDisks Large Homolog 4 ProteinDlg4 protein, ratIntracellular Signaling Peptides and ProteinsMembrane ProteinsPTEN PhosphohydrolasePten protein, ratReceptors, AMPAReceptors, N-Methyl-D-Aspartate

Identifiers

PMID20628354
PMCPMC2924645
OpenAlexW1986287316

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.