Evidence map›Paper›PMID 27833846›Full record

ArticleFEBS open bio2016

Mesenchymal stromal cells derived from whole human umbilical cord exhibit similar properties to those derived from Wharton's jelly and bone marrow.

Claire Mennan, Sharon Brown, Helen McCarthy, Eleni Mavrogonatou, Dimitris Kletsas, John Garcia, Birender Balain, James Richardson, Sally Roberts

Abstract read
In one paragraph

Article in FEBS open bio, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

  1. Trial
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  3. Article
  4. Article
  5. Evaluation of mesenchymal stem cells as anFrontiers in cell and developmental biology · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Cell therapy for cartilage repair.Emerging topics in life sciences · 2021
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

9 authors.

Claire MennanThe Robert Jones & Agnes Hunt Orthopaedic Hospital NHS Foundation Trust & Institute of Science & Technology in Medicine Keele University Oswestry Shropshire UK.
Sharon BrownThe Robert Jones & Agnes Hunt Orthopaedic Hospital NHS Foundation Trust & Institute of Science & Technology in Medicine Keele University Oswestry Shropshire UK.
Helen McCarthyThe Robert Jones & Agnes Hunt Orthopaedic Hospital NHS Foundation Trust & Institute of Science & Technology in Medicine Keele University Oswestry Shropshire UK.
Eleni MavrogonatouLaboratory of Cell Proliferation and Ageing Institute of Biosciences and Applications National Centre for Scientific Research "Demokritos" Athens Greece.
Dimitris KletsasLaboratory of Cell Proliferation and Ageing Institute of Biosciences and Applications National Centre for Scientific Research "Demokritos" Athens Greece.
John GarciaThe Robert Jones & Agnes Hunt Orthopaedic Hospital NHS Foundation Trust & Institute of Science & Technology in Medicine Keele University Oswestry Shropshire UK.
Birender BalainThe Robert Jones & Agnes Hunt Orthopaedic Hospital NHS Foundation Trust & Institute of Science & Technology in Medicine Keele University Oswestry Shropshire UK.
James RichardsonThe Robert Jones & Agnes Hunt Orthopaedic Hospital NHS Foundation Trust & Institute of Science & Technology in Medicine Keele University Oswestry Shropshire UK.
Sally RobertsThe Robert Jones & Agnes Hunt Orthopaedic Hospital NHS Foundation Trust & Institute of Science & Technology in Medicine Keele University Oswestry Shropshire UK.

Funding

Arthritis Research UK 20253Medical Research Council MR/L010453/1Versus Arthritis 18480Versus Arthritis 19429
6 · The paper itself

Abstract

Mesenchymal stromal cells (MSC) can be isolated from several regions of human umbilical cords, including Wharton's jelly (WJ), artery, vein or cord lining. These MSC appear to be immune privileged and are promising candidates for cell therapy. However, isolating MSC from WJ, artery, vein or cord lining requires time-consuming tissue dissection. MSC can be obtained easily via briefly digesting complete segments of the umbilical cord, likely containing heterogenous or mixed populations of MSC (MC-MSC). MC-MSC are generally less well characterized than WJ-MSC, but nevertheless represent a potentially valuable population of MSC. This study aimed to further characterize MC-MSC in comparison to WJ-MSC and also the better-characterized bone marrow-derived MSC (BM-MSC). MC-MSC proliferated faster, with significantly faster doubling times reaching passage one 8.8 days sooner and surviving longer in culture than WJ-MSC. All MSC retained the safety aspect of reducing telomere length with increasing passage number. MSC were also assessed for their ability to suppress T-cell proliferation and for the production of key markers of pluripotency, embryonic stem cells, tolerogenicity (CD40, CD80, CD86 and HLA-DR) and immunomodulation (indoleamine 2,3-dioxygenase [IDO] and HLA-G). The MC-MSC population displayed all of the positive attributes of WJ-MSC and BM-MSC, but they were more efficient to obtain and underwent more population doublings than from WJ, suggesting that MC-MSC are promising candidates for allogeneic cell therapy in regenerative medicine.

Indexed as

allogeneic cell therapybone marrow‐derived mesenchymal stromal cellsimmunomodulationumbilical cord‐derived mesenchymal stromal cells

Identifiers

PMID27833846
PMCPMC5095143

What OpenQuestion holds

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Registered trials

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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.