Evidence map›Paper›PMID 28968740›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2017

Activity-Dependent Neuroplasticity Induced by an Enriched Environment Reverses Cognitive Deficits in Scribble Deficient Mouse.

Muna L Hilal, Maité M Moreau, Claudia Racca, Vera L Pinheiro, Nicolas H Piguel, Marie-Josée Santoni, Steve Dos Santos Carvalho, Jean-Michel Blanc, Yah-Se K Abada, Ronan Peyroutou and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2017. 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
0.9field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Neuron-Specific Deletion ofFrontiers in genetics · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. 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

20 authors at 6 institutions in 3 countries.

Muna L HilalINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Maité M MoreauINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Claudia RaccaInstitute of Neuroscience, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Vera L PinheiroINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Nicolas H PiguelINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Marie-Josée SantoniCRCM, INSERM U1068, F-13009 Marseille, France.
Steve Dos Santos CarvalhoINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Jean-Michel BlancINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Yah-Se K AbadaINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Ronan PeyroutouINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Chantal MedinaINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Hélène DoatINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Thomas PapouinINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Laurent VuillardBioXtal Structural Biology Unit, Campus de Luminy, F-13288 Marseille, France.
Jean-Paul BorgCRCM, INSERM U1068, F-13009 Marseille, France.
Rivka RachelMouse Cancer Genetics Program, National Cancer Institute-Frederick, Frederick, Maryland 21702, USA.
Aude PanatierINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Mireille MontcouquiolINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Stéphane H R OlietINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Nathalie SansINSERM, Neurocentre Magendie, Unité U1215, F-33000 Bordeaux, France.
Neurocentre Magendie · FRUniversité de Bordeaux · FRInserm · FRCentre National de la Recherche Scientifique · FRCancer Genetics (United States) · USNewcastle University · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Planar cell polarity (PCP) signaling is well known to play a critical role during prenatal brain development; whether it plays specific roles at postnatal stages remains rather unknown. Here, we investigated the role of a key PCP-associated gene scrib in CA1 hippocampal structure and function at postnatal stages. We found that Scrib is required for learning and memory consolidation in the Morris water maze as well as synaptic maturation and NMDAR-dependent bidirectional plasticity. Furthermore, we unveiled a direct molecular interaction between Scrib and PP1/PP2A phosphatases whose levels were decreased in postsynaptic density of conditional knock-out mice. Remarkably, exposure to enriched environment (EE) preserved memory formation in CaMK-Scrib-/- mice by recovering synaptic plasticity and maturation. Thus, Scrib is required for synaptic function involved in memory formation and EE has beneficiary therapeutic effects. Our results demonstrate a distinct new role for a PCP-associated protein, beyond embryonic development, in cognitive functions during adulthood.

Indexed as

EnvironmentAnimalsChlorocebus aethiopsCognitive DysfunctionCOS CellsHippocampusHousing, AnimalIntracellular Signaling Peptides and ProteinsLearning DisabilitiesMaleMemory DisordersMice, KnockoutModels, MolecularNeuronal PlasticityPost-Synaptic DensityReceptors, N-Methyl-D-AspartateIntracellular Signaling Peptides and ProteinsReceptors, N-Methyl-D-Aspartatescrib protein, mouseconsolidation memoryLTDphosphatasesplanar cell polaritysynapse

Identifiers

PMID28968740
PMCPMC5939200
OpenAlexW2549504385

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.