Evidence map›Paper›PMID 21292011›Full record

ArticleMolecular and cellular neurosciences2011

NG2 cells are uniformly distributed and NG2 is not required for barrel formation in the somatosensory cortex.

Robert A Hill, Rie Natsume, Kenji Sakimura, Akiko Nishiyama

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular neurosciences, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Role of Chondroitin Sulfate Proteoglycans in Nervous System Development.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Review
  5. Article
  6. Myelin plasticity in adulthood and aging.Neuroscience letters · 2020
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. NG2 cells in white matter but not gray matter proliferate in response to PDGF.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  14. 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

4 authors at 2 institutions in 2 countries.

Robert A HillDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, CT 06269, USA.
Rie Natsume
Kenji Sakimura
Akiko Nishiyama
Niigata University · JPUniversity of Connecticut · US

Funding

Mechanisms of axon-NG2 cell interactionR01NS049267 · NINDS · UNIVERSITY OF CONNECTICUT STORRS · PI NISHIYAMA, AKIKO · 2005 to 2008
$1.3M
NINDS NIH HHS R01 NS049267
6 · The paper itself

Abstract

The somatosensory barrel cortex in the rodent forms during the first postnatal week setting up a periphery related map with each whisker represented as a bundle of thalamocortical axons (TCAs) in layer IV. The centers of each barrel (hollows) contain the densely packed TCAs, while the areas between each barrel (septa) form a boundary between each barrel. NG2 chondroitin sulfate proteoglycan (CSPG) expressing cells (NG2 cells, polydendrocytes) make up a unique population of glial cells that receive synaptic like input and form close contacts with growing axons. In the present study we investigated the developmental distribution of NG2 cells in the barrel cortex to determine if they display preferential septa distribution similar to other extracellular and cell surface CSPGs. Immunohistochemistry for NG2 and platelet-derived growth factor receptor alpha (PDGFRα) in NG2DsRedBAC transgenic mice showed uniform distribution of NG2 cells and processes in barrel hollows and septa at postnatal (P) days 5, 6, 7, 8, 14, and 30. Changes in the barrel pattern formation caused by cauterization of one row of whiskers at P1 resulted in corresponding changes in extracellular and cell surface CSPG distribution at P7 but no detectable changes in NG2 cell bodies and processes. Furthermore, no abnormalities in barrel formation or reorganization were detected in NG2 knockout mice. These observations suggest that NG2 cells are unlikely to play an inhibitory boundary role on TCA growth and that NG2 expression is not necessary for normal barrel formation.

Indexed as

AnimalsAntigensBiomarkersChondroitin Sulfate Proteoglycan 4MiceMice, Inbred C57BLMice, KnockoutNeuronsProteoglycansRatsRats, Sprague-DawleyRecombinant Fusion ProteinsSomatosensory CortexVibrissaeAntigensBiomarkersChondroitin Sulfate Proteoglycan 4ProteoglycansRecombinant Fusion Proteins

Identifiers

PMID21292011
PMCPMC3068479
OpenAlexW2037175660

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.