Evidence map›Paper›PMID 26309136›Full record

ArticleThe European journal of neuroscience2016

Human Schwann-like cells derived from adipose-derived mesenchymal stem cells rapidly de-differentiate in the absence of stimulating medium.

Alessandro Faroni, Richard J P Smith, Li Lu, Adam J Reid

Open access · hybridAbstract read
In one paragraph

Article in The European journal of neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. Combinatorial expression of glial transcription factors induces Schwann cell-specific gene expression in mouse embryonic fibroblasts.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  3. Peripheral nerve repair: innovations and future directions.Journal of translational medicine · 2026
    Review
  4. Review
  5. [Research progress in auxiliary components of nerve conduit for treating peripheral nerve injuries].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2025
    Review
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  10. Review
  11. Article
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  13. Article
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  19. Recent Stem Cell Research on Hemorrhagic Stroke : An Update.Journal of Korean Neurosurgical Society · 2022
    Article
  20. Review
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 1 institution in 2 countries.

Alessandro FaroniBlond McIndoe Laboratories, Stopford Building, Centre for Tissue Injury and Repair, Institute of Inflammation and Repair, University of Manchester, Oxford Road, Manchester, M13 9PT, UK.
Richard J P SmithBlond McIndoe Laboratories, Stopford Building, Centre for Tissue Injury and Repair, Institute of Inflammation and Repair, University of Manchester, Oxford Road, Manchester, M13 9PT, UK.
Li LuBlond McIndoe Laboratories, Stopford Building, Centre for Tissue Injury and Repair, Institute of Inflammation and Repair, University of Manchester, Oxford Road, Manchester, M13 9PT, UK.
Adam J ReidBlond McIndoe Laboratories, Stopford Building, Centre for Tissue Injury and Repair, Institute of Inflammation and Repair, University of Manchester, Oxford Road, Manchester, M13 9PT, UK.ORCID http://orcid.org/0000-0003-1752-3302
University of Manchester · GB

Funding

Department of Health II-LA-0313-20003Medical Research Council MR/L011840/1
6 · The paper itself

Abstract

Finding a viable cell-based therapy to address peripheral nerve injury holds promise for enhancing the currently suboptimal microsurgical approaches to peripheral nerve repair. Autologous nerve grafting is the current gold standard for surgical repair of nerve gaps; however, this causes donor nerve morbidity in the patient, and the results remain unsatisfactory. Transplanting autologous Schwann cells (SCs) results in similar morbidity, as well as limited cell numbers and restricted potential for expansion in vitro. Adipose-derived stem cells (ASCs), 'differentiated' towards an SC-like phenotype in vitro (dASCs), have been presented as an alternative to SC therapies. The differentiation protocol stimulates ASCs to mimic the SC phenotype; however, the efficacy of dASCs in nerve repair is not yet convincing, and the practicality of the SC-like phenotype is unproven. Here, we examined the stability of dASCs by withdrawing differentiation medium for 72 h after the full 18-day differentiation protocol, and measuring changes in morphology, gene expression, and protein levels. Withdrawal of differentiation medium from dASCs resulted in a rapid reversion to stem cell-like characteristics. Quantitative real-time polymerase chain reaction and enzyme-linked immunosorbent assay analyses demonstrated a significant reduction in gene and protein expression of growth factors that were expressed at high levels following 'differentiation'. Therefore, we question the relevance of differentiation to an SC-like phenotype, as withdrawal of differentiation medium, a model of transplantation into an injured nerve, results in rapid reversion of the dASC phenotype to stem cell-like characteristics. Further investigation into the differentiation process and the response of dASCs to an injured environment must be undertaken prior to the use of dASCs in peripheral nerve repair therapies.

Indexed as

Cell DifferentiationAdipose TissueAdultCells, CulturedCulture MediaFemaleHumansIntercellular Signaling Peptides and ProteinsMesenchymal Stem CellsMiddle AgedSchwann CellsCulture MediaIntercellular Signaling Peptides and Proteinscell differentiationgrowth factorsperipheral nerve injuryperipheral nerve regeneration

Identifiers

PMID26309136
PMCPMC4744694
OpenAlexW2114721953

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.