Evidence map›Paper›PMID 26561800›Full record

ArticleInternational journal of molecular sciences2015

Connexin 50 Expression in Ependymal Stem Progenitor Cells after Spinal Cord Injury Activation.

Francisco Javier Rodriguez-Jimenez, Ana Alastrue-Agudo, Miodrag Stojkovic, Slaven Erceg, Victoria Moreno-Manzano

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Genetic association ofTranslational pediatrics · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Stem Cells Therapy for Spinal Cord Injury.International journal of molecular sciences · 2018
    Review
  11. Stem Cells and Labeling for Spinal Cord Injury.International journal of molecular sciences · 2016
    Review
  12. Stem Cell Activation in Adult Organisms.International journal of molecular sciences · 2016
    Article
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

5 authors at 2 institutions in 2 countries.

Francisco Javier Rodriguez-JimenezNeuronal and Tissue Regeneration Laboratory, Centro de Investigación Príncipe Felipe, Valencia E-46012, Spain. frodriguez@cipf.es.
Ana Alastrue-AgudoNeuronal and Tissue Regeneration Laboratory, Centro de Investigación Príncipe Felipe, Valencia E-46012, Spain. aalastrue@cipf.es.
Miodrag StojkovicSpebo Medical, 16000 Leskovac, Serbia. mstojkovic@spebo.co.rs.
Slaven ErcegStem Cell Therapies in Neurodegenerative Diseases Laboratory, Centro de Investigación Príncipe Felipe, Valencia E-46012, Spain. serceg@cipf.es.
Victoria Moreno-ManzanoNeuronal and Tissue Regeneration Laboratory, Centro de Investigación Príncipe Felipe, Valencia E-46012, Spain. vmorenom@cipf.es.
Centro de Investigacion Principe Felipe · ESUniversity of Kragujevac · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ion channels included in the family of Connexins (Cx) help to control cell proliferation and differentiation of neuronal progenitors. Here we explored the role of Connexin 50 (Cx50) in cell fate modulation of adult spinal cord derived neural precursors located in the ependymal canal (epSPC). epSPC from non-injured animals showed high expression levels of Cx50 compared to epSPC from animals with spinal cord injury (SCI) (epSPCi). When epSPC or epSPCi were induced to spontaneously differentiate in vitro we found that Cx50 favors glial cell fate, since higher expression levels, endogenous or by over-expression of Cx50, augmented the expression of the astrocyte marker GFAP and impaired the neuronal marker Tuj1. Cx50 was found in both the cytoplasm and nucleus of glial cells, astrocytes and oligodendrocyte-derived cells. Similar expression patterns were found in primary cultures of mature astrocytes. In addition, opposite expression profile for nuclear Cx50 was observed when epSPC and activated epSPCi were conducted to differentiate into mature oligodendrocytes, suggesting a different role for this ion channel in spinal cord beyond cell-to-cell communication. In vivo detection of Cx50 by immunohistochemistry showed a defined location in gray matter in non-injured tissues and at the epicenter of the injury after SCI. epSPCi transplantation, which accelerates locomotion regeneration by a neuroprotective effect after acute SCI is associated with a lower signal of Cx50 within the injured area, suggesting a minor or detrimental contribution of this ion channel in spinal cord regeneration by activated epSPCi.

Indexed as

Cell DifferentiationStem Cell TransplantationAnimalsAstrocytesCell NucleusCell ProliferationConnexin 50ConnexinsCytoplasmEpendymaFemaleGene Expression RegulationGlial Fibrillary Acidic ProteinNeural Stem CellsNeurogliaNeuronsConnexin 50ConnexinsGlial Fibrillary Acidic ProteinTubb3 protein, ratTubulinconnexinsependymal stem progenitor cellsspinal cord

Identifiers

PMID26561800
PMCPMC4661840
OpenAlexW2116866426

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.