Evidence map›Paper›PMID 25708702›Full record

ArticleCellular and molecular life sciences : CMLS2015

Increased migration of olfactory ensheathing cells secreting the Nogo receptor ectodomain over inhibitory substrates and lesioned spinal cord.

Diego Reginensi, Patricia Carulla, Sara Nocentini, Oscar Seira, Xavier Serra-Picamal, Abel Torres-Espín, Andreu Matamoros-Angles, Rosalina Gavín, María Teresa Moreno-Flores, Francisco Wandosell and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Olfactory Ensheathing Cell-Conditioned Medium Reverts AβCellular and molecular neurobiology · 2017
    Article
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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

14 authors at 7 institutions in 2 countries.

Diego ReginensiMolecular and Cellular Neurobiotechnology, Institute of Bioengineering of Catalonia (IBEC), Parc Científic de Barcelona, Baldiri Reixac 15-12, 08028, Barcelona, Spain.
Patricia Carulla
Sara Nocentini
Oscar Seira
Xavier Serra-Picamal
Abel Torres-Espín
Andreu Matamoros-Angles
Rosalina Gavín
María Teresa Moreno-Flores
Francisco Wandosell
Josep Samitier
Xavier Trepat
Xavier Navarro
José Antonio del Río
Institute for Bioengineering of Catalonia · ESBiomedical Research Networking Center on Neurodegenerative Diseases · ESUniversidad Francisco de Vitoria · ESCentro de Biología Molecular Severo Ochoa · ESInstitució Catalana de Recerca i Estudis Avançats · ESUniversidad Autónoma de Madrid · ESUniversitat de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Olfactory ensheathing cell (OEC) transplantation emerged some years ago as a promising therapeutic strategy to repair injured spinal cord. However, inhibitory molecules are present for long periods of time in lesioned spinal cord, inhibiting both OEC migration and axonal regrowth. Two families of these molecules, chondroitin sulphate proteoglycans (CSPG) and myelin-derived inhibitors (MAIs), are able to trigger inhibitory responses in lesioned axons. Mounting evidence suggests that OEC migration is inhibited by myelin. Here we demonstrate that OEC migration is largely inhibited by CSPGs and that inhibition can be overcome by the bacterial enzyme Chondroitinase ABC. In parallel, we have generated a stable OEC cell line overexpressing the Nogo receptor (NgR) ectodomain to reduce MAI-associated inhibition in vitro and in vivo. Results indicate that engineered cells migrate longer distances than unmodified OECs over myelin or oligodendrocyte-myelin glycoprotein (OMgp)-coated substrates. In addition, they also show improved migration in lesioned spinal cord. Our results provide new insights toward the improvement of the mechanisms of action and optimization of OEC-based cell therapy for spinal cord lesion.

Indexed as

AnimalsAxonsCell MovementCells, CulturedChondroitin Sulfate ProteoglycansCloning, MolecularGPI-Linked ProteinsMicrofluidic Analytical TechniquesMyelin ProteinsMyelin SheathNerve RegenerationNeurogliaNogo Receptor 1Olfactory BulbOligodendrocyte-Myelin GlycoproteinProtein Structure, TertiaryChondroitin Sulfate ProteoglycansGPI-Linked ProteinsMyelin ProteinsNogo Receptor 1Oligodendrocyte-Myelin GlycoproteinReceptors, Cell SurfaceRtn4r protein, rat

Identifiers

PMID25708702
PMCPMC11113838
OpenAlexW2033193090

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.