Evidence map›Paper›PMID 24604282›Full record

Trial reportStem cells translational medicine2014

Isolation of neural progenitor cells from the human adult subventricular zone based on expression of the cell surface marker CD271.

Miriam E van Strien, Jacqueline A Sluijs, Brent A Reynolds, Dennis A Steindler, Eleonora Aronica, Elly M Hol

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Stem cells translational medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 47 citations in OpenAlex.

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  13. New GFAP splice isoform (GFAPµ) differentially expressed in glioma translates into 21 kDa N-terminal GFAP protein.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
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  14. Review
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  16. The optic nerve lamina region is a neural progenitor cell niche.Proceedings of the National Academy of Sciences of the United States of America · 2020
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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

6 authors at 5 institutions in 2 countries.

Miriam E van StrienDepartment of Astrocyte Biology and Neurodegeneration, The Netherlands Institute for Neuroscience, an Institute of the Royal Netherlands Academy of Sciences, Amsterdam, The Netherlands; Department of Neurosurgery, McKnight Brain Institute, University of Florida, Gainesville, Florida, USA; Department of Neuropathology, Academic Medical Center, Amsterdam, The Netherlands; Swammerdam Institute for Life Sciences, Center for Neuroscience, University of Amsterdam, Amsterdam, The Netherlands; Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center, Utrecht, The Netherlands.
Jacqueline A Sluijs
Brent A Reynolds
Dennis A Steindler
Eleonora Aronica
Elly M Hol
Royal Netherlands Academy of Arts and Sciences · NLAcademic Medical Center · NLNetherlands Institute for Neuroscience · NLUniversity Medical Center Utrecht · NLUniversity of Florida · US

Funding

STEM/PROGENITOR CELL PROTECTION FOR PARKINSON'S DISEASER01NS055165 · NINDS · UNIVERSITY OF FLORIDA · PI STEINDLER, DENNIS A. · 2007 to 2011
$1.6M
NINDS NIH HHS NS055165NINDS NIH HHS R01 NS055165
6 · The paper itself

Abstract

Neural progenitor cells (NPCs) in the subventricular zone (SVZ) hold promise for future therapy for neurodegenerative disorders, because the stimulation of adult neurogenesis could potentially restore the function of degenerating neurons and glia. To obtain more knowledge on these NPCs, we developed a method to specifically isolate NPCs from postmortem adult human brains based on the expression of the specific human adult neural stem/progenitor cell marker glial fibrillary acidic protein δ (GFAPδ). An extensive immunophenotyping analysis for cell surface markers resulted in the observation that CD271 was limited to the SVZ-derived GFAPδ-positive cells. CD271(+) cells developed into neurospheres and could be differentiated into astrocytes, neurons, and oligodendrocytes. We are the first to show that a pure population of NPCs can be isolated from the adult human SVZ, which is highly instrumental for developing future therapies based on stimulating endogenous SVZ neurogenesis.

Indexed as

BrainCell SeparationGene ExpressionNeural Stem CellsAdultAntigens, DifferentiationAstrocytesCell DifferentiationFemaleGlial Fibrillary Acidic ProteinHumansMaleNerve Tissue ProteinsNeurogenesisNeuronsOligodendrogliaAntigens, DifferentiationGlial Fibrillary Acidic ProteinNerve Tissue ProteinsNGFR protein, humanReceptors, Nerve Growth FactorGlial fibrillary acidic protein deltaHuman adult neural progenitor cellsNeurodegenerative disordersSpecific isolationSubventricular zone

Identifiers

PMID24604282
PMCPMC3973708
OpenAlexW2160625834

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.