Evidence map›Paper›PMID 26530515›Full record

ArticleStem cell research & therapy2015

Adult bone marrow mesenchymal and neural crest stem cells are chemoattractive and accelerate motor recovery in a mouse model of spinal cord injury.

Virginie Neirinckx, Gulistan Agirman, Cécile Coste, Alice Marquet, Valérie Dion, Bernard Rogister, Rachelle Franzen, Sabine Wislet

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2015. 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 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Role of Stem Cell-Derived Exosomes and microRNAs in Spinal Cord Injury.International journal of molecular sciences · 2023
    Review
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  9. Gene-modified leucoconcentrate for personalizedNeural regeneration research · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Virginie NeirinckxGroupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Neurosciences Research Center, Unit of Nervous system disorders and treatment, University of Liège, Tour de Pathologie 2, Avenue de l'Hôpital, 1, 4000, Liège, Belgium. Virginie.Neirinckx@ulg.ac.be.
Gulistan AgirmanGroupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Neurosciences Research Center, Unit of Nervous system disorders and treatment, University of Liège, Tour de Pathologie 2, Avenue de l'Hôpital, 1, 4000, Liège, Belgium. g.agirman@student.ulg.ac.be.
Cécile CosteGroupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Neurosciences Research Center, Unit of Nervous system disorders and treatment, University of Liège, Tour de Pathologie 2, Avenue de l'Hôpital, 1, 4000, Liège, Belgium. Cecile.Coste@ulg.ac.be.
Alice MarquetGroupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Neurosciences Research Center, Unit of Nervous system disorders and treatment, University of Liège, Tour de Pathologie 2, Avenue de l'Hôpital, 1, 4000, Liège, Belgium. Alice.Marquet@ulg.ac.be.
Valérie DionGroupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Neurosciences Research Center, Unit of Nervous system disorders and treatment, University of Liège, Tour de Pathologie 2, Avenue de l'Hôpital, 1, 4000, Liège, Belgium. v.dion@ulg.ac.be.
Bernard RogisterGroupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Neurosciences Research Center, Unit of Nervous system disorders and treatment, University of Liège, Tour de Pathologie 2, Avenue de l'Hôpital, 1, 4000, Liège, Belgium. Bernard.Rogister@ulg.ac.be.
Rachelle FranzenGroupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Neurosciences Research Center, Unit of Nervous system disorders and treatment, University of Liège, Tour de Pathologie 2, Avenue de l'Hôpital, 1, 4000, Liège, Belgium. rfranzen@ulg.ac.be.
Sabine WisletGroupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Neurosciences Research Center, Unit of Nervous system disorders and treatment, University of Liège, Tour de Pathologie 2, Avenue de l'Hôpital, 1, 4000, Liège, Belgium. s.wislet@ulg.ac.be.
University of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionStem cells from adult tissues were considered for a long time as promising tools for regenerative therapy of neurological diseases, including spinal cord injuries (SCI). Indeed, mesenchymal (MSCs) and neural crest stem cells (NCSCs) together constitute the bone marrow stromal stem cells (BMSCs) that were used as therapeutic options in various models of experimental SCI. However, as clinical approaches remained disappointing, we thought that reducing BMSC heterogeneity should be a potential way to improve treatment efficiency and reproducibility.

methodsWe investigated the impact of pure populations of MSCs and NCSCs isolated from adult bone marrow in a mouse model of spinal cord injury. We then analyzed the secretome of both MSCs and NCSCs, and its effect on macrophage migration in vitro.

resultsWe first observed that both cell types induced motor recovery in mice, and modified the inflammatory reaction in the lesion site. We also demonstrated that NCSCs but especially MSCs were able to secrete chemokines and attract macrophages in vitro. Finally, it appears that MSC injection in the spinal cord enhance early inflammatory events in the blood and spinal cord of SCI mice.

conclusionsAltogether, our results suggest that both cell types have beneficial effects in experimental SCI, and that further investigation should be dedicated to the regulation of the inflammatory reaction following SCI, in the context of stem cell-based therapy but also in the early-phase clinical management of SCI patients.

Indexed as

ChemotaxisMesenchymal Stem Cell TransplantationAnimalsChemokinesFemaleMesenchymal Stem CellsMiceMice, Inbred C57BLMice, TransgenicMotor ActivityNerve RegenerationNeural CrestNeural Stem CellsRAW 264.7 CellsRecovery of FunctionRegenerative MedicineChemokines

Identifiers

PMID26530515
PMCPMC4632651
OpenAlexW2192916530

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.