Evidence map›Paper›PMID 27171265›Full record

ArticleCell death & disease2016

Intraventricular injections of mesenchymal stem cells activate endogenous functional remyelination in a chronic demyelinating murine model.

P Cruz-Martinez, S González-Granero, M M Molina-Navarro, J Pacheco-Torres, J M García-Verdugo, E Geijo-Barrientos, J Jones, S Martinez

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Overexpression ofCurrent issues in molecular biology · 2023
    Article
  5. Review
  6. Remyelination in Multiple Sclerosis: Findings in the Cuprizone Model.International journal of molecular sciences · 2022
    Review
  7. Article
  8. Recent Stem Cell Research on Hemorrhagic Stroke : An Update.Journal of Korean Neurosurgical Society · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

P Cruz-MartinezNeuroscience Institute, University Miguel Hernández - Spanish Council for Scientific Research (UMH-CSIC), Alicante, Spain.
S González-GraneroLaboratorio de Neurobiología Comparada, Instituto Cavanilles, Universidad de Valencia, CIBERNED, Valencia, Spain.
M M Molina-NavarroLaboratorio de Neurobiología Comparada, Instituto Cavanilles, Universidad de Valencia, CIBERNED, Valencia, Spain.
J Pacheco-TorresNeuroscience Institute, University Miguel Hernández - Spanish Council for Scientific Research (UMH-CSIC), Alicante, Spain.
J M García-VerdugoLaboratorio de Neurobiología Comparada, Instituto Cavanilles, Universidad de Valencia, CIBERNED, Valencia, Spain.
E Geijo-BarrientosNeuroscience Institute, University Miguel Hernández - Spanish Council for Scientific Research (UMH-CSIC), Alicante, Spain.
J JonesNeuroscience Institute, University Miguel Hernández - Spanish Council for Scientific Research (UMH-CSIC), Alicante, Spain.
S MartinezNeuroscience Institute, University Miguel Hernández - Spanish Council for Scientific Research (UMH-CSIC), Alicante, Spain.
Universitat de Miguel Hernández d'Elx · ESUniversitat de València · ESUniversidad de Murcia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current treatments for demyelinating diseases are generally only capable of ameliorating the symptoms, with little to no effect in decreasing myelin loss nor promoting functional recovery. Mesenchymal stem cells (MSCs) have been shown by many researchers to be a potential therapeutic tool in treating various neurodegenerative diseases, including demyelinating disorders. However, in the majority of the cases, the effect was only observed locally, in the area surrounding the graft. Thus, in order to achieve general remyelination in various brain structures simultaneously, bone marrow-derived MSCs were transplanted into the lateral ventricles (LVs) of the cuprizone murine model. In this manner, the cells may secrete soluble factors into the cerebrospinal fluid (CSF) and boost the endogenous oligodendrogenic potential of the subventricular zone (SVZ). As a result, oligodendrocyte progenitor cells (OPCs) were recruited within the corpus callosum (CC) over time, correlating with an increased myelin content. Electrophysiological studies, together with electron microscopy (EM) analysis, indicated that the newly formed myelin correctly enveloped the demyelinated axons and increased signal transduction through the CC. Moreover, increased neural stem progenitor cell (NSPC) proliferation was observed in the SVZ, possibly due to the tropic factors released by the MSCs. In conclusion, the findings of this study revealed that intraventricular injections of MSCs is a feasible method to elicit a paracrine effect in the oligodendrogenic niche of the SVZ, which is prone to respond to the factors secreted into the CSF and therefore promoting oligodendrogenesis and functional remyelination.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsBone Marrow CellsCell- and Tissue-Based TherapyCell DifferentiationCorpus CallosumCuprizoneDemyelinating DiseasesDisease Models, AnimalGene ExpressionHumansInjections, IntraventricularIntercellular Signaling Peptides and ProteinsLateral VentriclesMesenchymal Stem CellsMiceCuprizoneIntercellular Signaling Peptides and Proteins

Identifiers

PMID27171265
PMCPMC4917663
OpenAlexW4232505466

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.