Evidence map›Paper›PMID 25083703›Full record

ArticlePloS one2014

Deletion of the NMDA receptor GluN2A subunit significantly decreases dendritic growth in maturing dentate granule neurons.

Timal S Kannangara, Crystal A Bostrom, Andrea Ratzlaff, Lee Thompson, Robyn M Cater, Joana Gil-Mohapel, Brian R Christie

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Timal S KannangaraDivision of Medical Sciences, University of Victoria, Victoria, Canada; Department of Cellular and Physiological Sciences, University of British Columbia, Victoria, Canada; Graduate Program of Neuroscience and The Brain Research Centre, University of British Columbia, Victoria, Canada.
Crystal A BostromDivision of Medical Sciences, University of Victoria, Victoria, Canada; Department of Biology, University of Victoria, Victoria, Canada.
Andrea RatzlaffDivision of Medical Sciences, University of Victoria, Victoria, Canada; Department of Biology, University of Victoria, Victoria, Canada.
Lee ThompsonDivision of Medical Sciences, University of Victoria, Victoria, Canada; Department of Biology, University of Victoria, Victoria, Canada.
Robyn M CaterDivision of Medical Sciences, University of Victoria, Victoria, Canada; Department of Biology, University of Victoria, Victoria, Canada.
Joana Gil-MohapelDivision of Medical Sciences, University of Victoria, Victoria, Canada.
Brian R ChristieDivision of Medical Sciences, University of Victoria, Victoria, Canada; Department of Biology, University of Victoria, Victoria, Canada; Neuroscience Graduate Program, University of Victoria, Victoria, Canada; Department of Cellular and Physiological Sciences, University of British Columbia, Victoria, Canada; Graduate Program of Neuroscience and The Brain Research Centre, University of British Columbia, Victoria, Canada.
University of Victoria · CA

Funding

Canadian Institutes of Health Research CIHR MOP 125888
6 · The paper itself

Abstract

It is known that NMDA receptors can modulate adult hippocampal neurogenesis, but the contribution of specific regulatory GluN2 subunits has been difficult to determine. Here we demonstrate that mice lacking GluN2A (formerly NR2A) do not show altered cell proliferation or neuronal differentiation, but present significant changes in neuronal morphology in dentate granule cells. Specifically, GluN2A deletion significantly decreased total dendritic length and dendritic complexity in DG neurons located in the inner granular zone. Furthermore, the absence of GluN2A also resulted in a localized increase in spine density in the middle molecular layer, a region innervated by the medial perforant path. Interestingly, alterations in dendritic morphology and spine density were never seen in dentate granule cells located in the outer granular zone, a region that has been hypothesized to contain older, more mature, neurons. These results indicate that although the GluN2A subunit is not critical for the cell proliferation and differentiation stages of the neurogenic process, it does appear to play a role in establishing synaptic and dendritic morphology in maturing dentate granule cells localized in the inner granular zone.

Indexed as

Gene DeletionAnimalsCell DifferentiationCell ProliferationDendritesDendritic SpinesDentate GyrusImmunohistochemistryMaleMiceMice, KnockoutNeurogenesisProtein SubunitsPyramidal CellsReceptors, N-Methyl-D-AspartateProtein SubunitsReceptors, N-Methyl-D-Aspartate

Identifiers

PMID25083703
PMCPMC4118862
OpenAlexW1978818962

What OpenQuestion holds

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LicenceCC BY
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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.