Evidence map›Paper›PMID 26684484›Full record

ArticleStem cell research & therapy2015

Tissues from equine cadaver ligaments up to 72 hours of post-mortem: a promising reservoir of stem cells.

Mohamad Khir Shikh Alsook, Annick Gabriel, Joëlle Piret, Olivier Waroux, Céline Tonus, Delphine Connan, Etienne Baise, Nadine Antoine

Open 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. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-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, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Cadaveric Adipose-Derived Stem Cells for Regenerative Medicine and Research.International journal of molecular sciences · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. 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

8 authors at 1 institution in 1 country.

Mohamad Khir Shikh AlsookAnatomy Unit, FARAH Research Center & Faculty of Veterinary Medicine, University of Liège, Liège, Belgium. mkal.sook@doct.ulg.ac.be.
Annick GabrielAnatomy Unit, FARAH Research Center & Faculty of Veterinary Medicine, University of Liège, Liège, Belgium. annick.gabriel@ulg.ac.be.
Joëlle PiretHistology Unit, FARAH Research Center & Faculty of Veterinary Medicine, University of Liège, Liège, Belgium. jpiret@ulg.ac.be.
Olivier WarouxHistology Unit, FARAH Research Center & Faculty of Veterinary Medicine, University of Liège, Liège, Belgium. o.waroux@ulg.ac.be.
Céline TonusEmbryology Unit, FARAH Research Center & Faculty of Veterinary Medicine, University of Liège, Liège, Belgium. ctonus@ulg.ac.be.
Delphine ConnanEmbryology Unit, GIGA-Development, Stem Cells and Regenerative Medicine and Faculty of Veterinary Medicine, University of Liège, Liège, Belgium. delphine.connan@ulg.ac.be.
Etienne BaiseFARAH Research Center & Faculty of Veterinary Medicine, University of Liège, Liège, Belgium. etienne.baise@ulg.ac.be.
Nadine AntoineHistology Unit, FARAH Research Center & Faculty of Veterinary Medicine, University of Liège, Liège, Belgium. nadine.antoine@ulg.ac.be.
University of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal stem cells (MSCs) harvested from cadaveric tissues represent a promising approach for regenerative medicine. To date, no study has investigated whether viable MSCs could survive in cadaveric tissues from tendon or ligament up to 72 hours of post-mortem. The purpose of the present work was to find out if viable MSCs could survive in cadaveric tissues from adult equine ligaments up to 72 hours of post-mortem, and to assess their ability (i) to remain in an undifferentiated state and (ii) to divide and proliferate in the absence of any specific stimulus.

methodsMSCs were isolated from equine cadaver (EC) suspensory ligaments within 48-72 hours of post-mortem. They were evaluated for viability, proliferation, capacity for tri-lineage differentiation, expression of cell surface markers (CD90, CD105, CD73, CD45), pluripotent transcription factor (OCT-4), stage-specific embryonic antigen-1 (SSEA-1), neuron-specific class III beta-tubulin (TUJ-1), and glial fibrillary acidic protein (GFAP). As well, they were characterized by transmission electron microscope (TEM).

resultsEC-MSCs were successfully isolated and maintained for 20 passages with high cell viability and proliferation. Phase contrast microscopy revealed that cells with fibroblast-like appearance were predominant in the culture. Differentiation assays proved that EC-MSCs are able to differentiate towards mesodermal lineages (osteogenic, adipogenic, chondrogenic). Flow cytometry analysis demonstrated that EC-MSCs expressed CD90, CD105, and CD73, while being negative for the leukocyte common antigen CD45. Immunofluorescence analysis showed a high percentage of positive cells for OCT-4 and SSEA-1. Surprisingly, in absence of any stimuli, some adherent cells closely resembling neuronal and glial morphology were also observed. Interestingly, our results revealed that approximately 15 % of the cell populations were TUJ-1 positive, whereas GFAP expression was detected in only a few cells. Furthermore, TEM analysis confirmed the stemness of EC-MSCs and identified some cells with a typical neuronal morphology.

conclusionsOur findings raise the prospect that the tissues harvested from equine ligaments up to 72 hours of post-mortem represent an available reservoir of specific stem cells. EC-MSCs could be a promising alternative source for tissue engineering and stem cell therapy in equine medicine.

Indexed as

AnimalsBiomarkersCadaverCell Culture TechniquesCell DifferentiationCell ProliferationCell SeparationGlial Fibrillary Acidic ProteinHorsesIn Vitro TechniquesLigamentsMesenchymal Stem CellsMicroscopy, Electron, TransmissionOctamer Transcription Factor-3Postmortem ChangesTime FactorsBiomarkersGlial Fibrillary Acidic ProteinOctamer Transcription Factor-3Tubulin

Identifiers

PMID26684484
PMCPMC4683699
OpenAlexW2197928945

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.