Evidence map›Paper›PMID 31038798›Full record

ArticleGlia2019

Aging restricts the ability of mesenchymal stem cells to promote the generation of oligodendrocytes during remyelination.

Francisco J Rivera, Alerie G de la Fuente, Chao Zhao, Maria E Silva, Ginez A Gonzalez, Roman Wodnar, Martina Feichtner, Simona Lange, Oihana Errea, Eleni Priglinger and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Glia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Mesenchymal Stem Cells in Cancer Therapy.Advances in experimental medicine and biology · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. DCXScientific reports · 2020
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Aging, Cellular Senescence, and Progressive Multiple Sclerosis.Frontiers in cellular neuroscience · 2020
    Review
  16. Therapeutic Potential of Mesenchymal Stem Cells for Cancer Therapy.Frontiers in bioengineering and biotechnology · 2020
    Review
  17. Article
  18. Article
  19. 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

22 authors at 5 institutions in 4 countries.

Francisco J RiveraLaboratory of Stem Cells and Neuroregeneration, Institute of Anatomy, Histology and Pathology, Faculty of Medicine, Universidad Austral de Chile, Valdivia, Chile.ORCID 0000-0001-7895-6318
Alerie G de la FuenteWellcome-MRC Cambridge Stem Cell Institute & Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0001-8366-4969
Chao ZhaoWellcome-MRC Cambridge Stem Cell Institute & Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0003-1144-1621
Maria E SilvaLaboratory of Stem Cells and Neuroregeneration, Institute of Anatomy, Histology and Pathology, Faculty of Medicine, Universidad Austral de Chile, Valdivia, Chile.ORCID 0000-0001-6236-7180
Ginez A GonzalezWellcome-MRC Cambridge Stem Cell Institute & Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0002-2146-9655
Roman WodnarInstitute of Molecular Regenerative Medicine, Paracelsus Medical University, Salzburg, Austria.
Martina FeichtnerInstitute of Molecular Regenerative Medicine, Paracelsus Medical University, Salzburg, Austria.
Simona LangeInstitute of Molecular Regenerative Medicine, Paracelsus Medical University, Salzburg, Austria.
Oihana ErreaWellcome-MRC Cambridge Stem Cell Institute & Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Eleni PriglingerInstitute of Molecular Regenerative Medicine, Paracelsus Medical University, Salzburg, Austria.ORCID 0000-0002-1484-0444
Anna O'SullivanInstitute of Molecular Regenerative Medicine, Paracelsus Medical University, Salzburg, Austria.
Pasquale RomanelliSpinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS), Paracelsus Medical University, Salzburg, Austria.ORCID 0000-0003-0874-6918
Janusz J JadaszLaboratory of Experimental Ophthalmology, Department of Ophthalmology, University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.ORCID 0000-0002-5505-4570
Gabriele BrachtlLaboratory for Immunological and Molecular Cancer Research, 3rd Medical Department for Hematology, Medical Oncology, Hemostasiology, Infectious Diseases, and Rheumatology, Federal Hospital of Salzburg and Paracelsus Medical University, Salzburg, Austria.
Richard GreilLaboratory for Immunological and Molecular Cancer Research, 3rd Medical Department for Hematology, Medical Oncology, Hemostasiology, Infectious Diseases, and Rheumatology, Federal Hospital of Salzburg and Paracelsus Medical University, Salzburg, Austria.
Herbert TempferSpinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS), Paracelsus Medical University, Salzburg, Austria.
Andreas TrawegerSpinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS), Paracelsus Medical University, Salzburg, Austria.ORCID 0000-0002-0220-4766
Luis F BátizCenter for Interdisciplinary Studies on the Nervous System (CISNe), Universidad Austral de Chile, Valdivia, Chile.ORCID 0000-0002-3043-8797
Patrick KüryDepartment of Neurology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.ORCID 0000-0002-2654-1126
Sebastien Couillard-DespresSpinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS), Paracelsus Medical University, Salzburg, Austria.ORCID 0000-0002-8486-6412
Robin J M FranklinWellcome-MRC Cambridge Stem Cell Institute & Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0001-6522-2104
Ludwig AignerInstitute of Molecular Regenerative Medicine, Paracelsus Medical University, Salzburg, Austria.ORCID 0000-0002-1653-8046
Paracelsus Medical University · ATWellcome/MRC Cambridge Stem Cell Institute · GBAustral University of Chile · CLDüsseldorf University Hospital · DEHeinrich Heine University Düsseldorf · DE

Funding

Medical Research Council G0300336Medical Research Council G0300338Medical Research Council G0700392Medical Research Council G0701476Medical Research Council G0802545Medical Research Council MC_PC_12009Medical Research Council MR/K008803/1Medical Research Council MR/M010503/1Wellcome Trust
6 · The paper itself

Abstract

Multiple sclerosis (MS) is a demyelinating disease of the central nervous system (CNS) that leads to severe neurological deficits. Due to their immunomodulatory and neuroprotective activities and their ability to promote the generation of oligodendrocytes, mesenchymal stem cells (MSCs) are currently being developed for autologous cell therapy in MS. As aging reduces the regenerative capacity of all tissues, it is of relevance to investigate whether MSCs retain their pro-oligodendrogenic activity with increasing age. We demonstrate that MSCs derived from aged rats have a reduced capacity to induce oligodendrocyte differentiation of adult CNS stem/progenitor cells. Aging also abolished the ability of MSCs to enhance the generation of myelin-like sheaths in demyelinated cerebellar slice cultures. Finally, in a rat model for CNS demyelination, aging suppressed the capability of systemically transplanted MSCs to boost oligodendrocyte progenitor cell (OPC) differentiation during remyelination. Thus, aging restricts the ability of MSCs to support the generation of oligodendrocytes and consequently inhibits their capacity to enhance the generation of myelin-like sheaths. These findings may impact on the design of therapies using autologous MSCs in older MS patients.

Indexed as

AgingAnimalsCells, CulturedDemyelinating DiseasesDisease Models, AnimalFemaleMaleMesenchymal Stem CellsOligodendrogliaRats, Inbred F344Rats, Sprague-DawleyRemyelinationTissue Culture Techniquesagingcell therapyCNS stem and progenitor cellsmesenchymal stem cellsmultiple sclerosisoligodendrocytesremyelination

Identifiers

PMID31038798
PMCPMC6618006
OpenAlexW2943606197

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.