Evidence map›Paper›PMID 24226267›Full record

ArticleJournal of neuropathology and experimental neurology2013

Oligodendrocyte lineage and subventricular zone response to traumatic axonal injury in the corpus callosum.

Genevieve M Sullivan, Amanda J Mierzwa, Naruchorn Kijpaisalratana, Haiying Tang, Yong Wang, Sheng-Kwei Song, Reed Selwyn, Regina C Armstrong

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.8field-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

55 citing papers in PubMed, 95 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

8 authors at 2 institutions in 1 country.

Genevieve M SullivanFrom the Program in Molecular and Cell Biology (GMS, RCA), Department of Anatomy (GMS, AJM, RCA), Physiology and Genetics, Center for Neuroscience and Regenerative Medicine (GMS, AJM, NK, HT, RS, RCA), Department of Radiology (HT, RS), Uniformed Services University of the Health Sciences, Bethesda, Maryland; Department of Radiology (YW, S-KS), Washington University, St. Louis, Missouri; and Department of Internal Medicine (NK), Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Amanda J Mierzwa
Naruchorn Kijpaisalratana
Haiying Tang
Yong Wang
Sheng-Kwei Song
Reed Selwyn
Regina C Armstrong
Uniformed Services University of the Health Sciences · USWashington University in St. Louis · US

Funding

PREDICTIVE VALUE OF DIFFUSION MRI IN CERVICAL SPONDYLOTIC MYELOPATHYR01NS047592 · NINDS · WASHINGTON UNIVERSITY · PI RAY, WILSON Z, SONG, SHENG-KWEI · 2005 to 2021
$5.8M
NINDS NIH HHS R01 NS047592NINDS NIH HHS R01-NS047592
6 · The paper itself

Abstract

Traumatic brain injury frequently causes traumatic axonal injury (TAI) in white matter tracts. Experimental TAI in the corpus callosum of adult mice was used to examine the effects on oligodendrocyte lineage cells and myelin in conjunction with neuroimaging. The injury targeted the corpus callosum over the subventricular zone, a source of neural stem/progenitor cells. Traumatic axonal injury was produced in the rostral body of the corpus callosum by impact onto the skull at the bregma. During the first week after injury, magnetic resonance diffusion tensor imaging showed that axial diffusivity decreased in the corpus callosum and that corresponding regions exhibited significant axon damage accompanied by hypertrophic microglia and reactive astrocytes. Oligodendrocyte progenitor proliferation increased in the subventricular zone and corpus callosum. Oligodendrocytes in the corpus callosum shifted toward upregulation of myelin gene transcription. Plp/CreER(T):R26IAP reporter mice showed normal reporter labeling of myelin sheaths 0 to 2 days after injury but labeling was increased between 2 and 7 days after injury. Electron microscopy revealed axon degeneration, demyelination, and redundant myelin figures. These findings expand the cell types and responses to white matter injuries that inform diffusion tensor imaging evaluation and identify pivotal white matter changes after TAI that may affect axon vulnerability vs. recovery after brain injury.

Indexed as

Adult Stem CellsAnimalsAntigensCell ProliferationCerebral VentriclesChondroitin Sulfate Proteoglycan 4Corpus CallosumCross-Sectional StudiesDiffuse Axonal InjuryDiffusion Magnetic Resonance ImagingDisease Models, AnimalGene Expression RegulationGlial Fibrillary Acidic ProteinLongitudinal StudiesMaleMembrane ProteinsAntigensChondroitin Sulfate Proteoglycan 4Glial Fibrillary Acidic ProteinMembrane ProteinsProteoglycansReceptors, Estrogen

Identifiers

PMID24226267
PMCPMC4130339
OpenAlexW1989217312

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.