Evidence map›Paper›PMID 28796246›Full record

ArticleCell death & disease2017

Identification and characterization of a new source of adult human neural progenitors.

Jinan Behnan, Biljana Stangeland, Tiziana Langella, Gaetano Finocchiaro, Giovanni Tringali, Torstein R Meling, Wayne Murrell

Abstract read
In one paragraph

Article in Cell death & disease, 2017. 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
–field-weighted citation impact
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.

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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.

Jinan BehnanDepartment of Immunology, Norwegian Center for Stem Cell Research, Institute of Clinical Medicine, Oslo University Hospital, Oslo, Norway.ORCID 0000-0001-5780-0971
Biljana StangelandDepartment of Immunology, Norwegian Center for Stem Cell Research, Institute of Clinical Medicine, Oslo University Hospital, Oslo, Norway.
Tiziana LangellaUnit of Molecular Neuro-Oncology, Neurological Institute C, Besta, Milan, Italy.
Gaetano FinocchiaroUnit of Molecular Neuro-Oncology, Neurological Institute C, Besta, Milan, Italy.
Giovanni TringaliDepartment of Neurosurgery, Neurological Institute C. Besta, Milan, Italy.
Torstein R MelingDepartment of Neurosurgery, Oslo University Hospital; Oslo, Norway.
Wayne MurrellVilhelm Magnus Laboratory of Neurosurgical Research, Institute for Surgical Research, Oslo University Hospital, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adult neural progenitor cells (aNPCs) are a potential source for cell based therapy for neurodegenerative diseases and traumatic brain injuries. These cells have been traditionally isolated from hippocampus, subventricular zone and white matter. However, there is still a need for an easily accessible source with better yield to counter the limitations of small surgical samples of previously characterized aNPCs. Here we show that ultrasonic aspirate (UA) samples currently considered as 'biological waste after surgery,' offer a good source for aNPCs. Furthermore, we show that culture conditions dictated the phenotype of cells across patients. The neurosphere-enriched cells were more similar to freshly isolated brain cells, while cells expanded adherently in serum conditions were similar to mesenchymal stem cells. However, cells expanded in these adherent conditions expressed some NPC and glial markers in addition to active canonical Wnt signaling. This suggests a mesenchymal-neuroectodermal hybrid nature of these cells. Finally, we show that UA-NPCs are comparable to those from neurogenic regions. Our findings suggest that UA samples can be used as a source for fresh and in vitro propagated aNPCs that could have various clinical applications.

Indexed as

Adult Stem CellsCell DifferentiationCells, CulturedFlow CytometryHippocampusHumansLateral VentriclesNeural Stem CellsNeurogenesisWhite MatterWnt Signaling Pathway

Identifiers

PMID28796246
PMCPMC5596556

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Registered trials

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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.