Evidence map›Paper›PMID 26295543›Full record

ArticleGlia2016

SSEA-4 and YKL-40 positive progenitor subtypes in the subventricular zone of developing human neocortex.

Christian B Brøchner, Kjeld Møllgård

Open access · hybridAbstract read
In one paragraph

Article in Glia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

7 citing papers in PubMed, 9 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

2 authors at 1 institution in 1 country.

Christian B BrøchnerDepartment of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3, Copenhagen, DK-2200, Denmark.
Kjeld MøllgårdDepartment of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3, Copenhagen, DK-2200, Denmark.
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The glycosphingolipid SSEA-4 and the glycoprotein YKL-40 have both been associated with human embryonic and neural stem cell differentiation. We investigated the distribution of SSEA-4 and YKL-40 positive cells in proliferative zones of human fetal forebrain using immunohistochemistry and double-labeling immunofluorescence. A few small rounded SSEA-4 and YKL-40 labeled cells were present in the radial glial BLBP positive proliferative zones adjacent to the lateral ganglionic eminence from 12th week post conception. With increasing age, a similarly stained cell population appeared more widespread in the subventricular zone. At midgestation, the entire subventricular zone showed patches of SSEA-4, YKL-40, and BLBP positive cells. Co-labeling with markers for radial glial cells (RGCs) and neuronal, glial, and microglial markers tested the lineage identity of this subpopulation of radial glial descendants. Adjacent to the ventricular zone, a minor fraction showed overlap with GFAP but not with nestin, Olig2, NG2, or S100. No co-localization was found with neuronal markers NeuN, calbindin, DCX or with markers for microglial cells (Iba-1, CD68). Moreover, the SSEA-4 and YKL-40 positive cell population in subventricular zone was largely devoid of Tbr2, a marker for intermediate neuronal progenitor cells descending from RGCs. YKL-40 has recently been found in astrocytes in the neuron-free fimbria, and both SSEA-4 and YKL-40 are present in malignant astroglial brain tumors. We suggest that the population of cells characterized by immunohistochemical combination of antibodies against SSEA-4 and YKL-40 and devoid of neuronal and microglial markers represent a yet unexplored astrogenic lineage illustrating the complexity of astroglial development.

Indexed as

AdipokinesAntigens, CDAntigens, Differentiation, MyelomonocyticAntigens, NuclearBasic Helix-Loop-Helix ProteinsCalbindinsCalcium-Binding ProteinsCarrier ProteinsCD68 MoleculeChitinase-3-Like Protein 1DNA-Binding ProteinsDoublecortin Domain ProteinsDoublecortin ProteinFatty Acid-Binding Protein 7HumansImmunohistochemistryAdipokinesAIF1 protein, humanAntigens, CDAntigens, Differentiation, MyelomonocyticAntigens, NuclearBasic Helix-Loop-Helix ProteinsCalbindinsCalcium-Binding ProteinsCarrier ProteinsCD68 antigen, humanCD68 MoleculeCHI3L1 protein, humanChitinase-3-Like Protein 1DCX protein, humanDNA-Binding ProteinsDoublecortin Domain ProteinsDoublecortin ProteinEOMES protein, humanFABP7 protein, humanFatty Acid-Binding Protein 7LectinsMicrofilament ProteinsMicrotubule-Associated ProteinsNerve Tissue ProteinsNES protein, humanNestinneuronal nuclear antigen NeuN, humanNeuropeptidesOLIG2 protein, humanOligodendrocyte Transcription Factor 2S100 Proteinsstage-specific embryonic antigen-4Stage-Specific Embryonic AntigensT-Box Domain ProteinsTumor Suppressor Proteinsastrocytescerebral cortexcorticogenesisdevelopmenthuman neural stem cells

Identifiers

PMID26295543
PMCPMC5049638
OpenAlexW2155646366

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.