Evidence map›Paper›PMID 28833807›Full record

ArticleStem cells (Dayton, Ohio)2017

The Wnt5a Receptor, Receptor Tyrosine Kinase-Like Orphan Receptor 2, Is a Predictive Cell Surface Marker of Human Mesenchymal Stem Cells with an Enhanced Capacity for Chondrogenic Differentiation.

Sally C Dickinson, Catherine A Sutton, Kyla Brady, Anna Salerno, Theoni Katopodi, Rhys L Williams, Christopher C West, Denis Evseenko, Ling Wu, Suzanna Pang and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. CD317Stem cell research & therapy · 2024
    Article
  9. Advances in Stem Cell-Based Therapies in the Treatment of Osteoarthritis.International journal of molecular sciences · 2023
    Review
  10. Review
  11. Article
  12. Cartilage Tissue Engineering: An Introduction.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  13. Article
  14. Blood Vessel Resident Human Stem Cells in Health and Disease.Stem cells translational medicine · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Running Against the Wnt: How Wnt/β-Catenin Suppresses Adipogenesis.Frontiers in cell and developmental biology · 2021
    Review
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

16 authors at 6 institutions in 2 countries.

Sally C DickinsonInstitute of Integrative Biology, University of Liverpool, United Kingdom.
Catherine A SuttonSchool of Cellular and Molecular Medicine, Faculty of Medical and Veterinary Sciences, University of Bristol, United Kingdom.
Kyla BradyInstitute of Integrative Biology, University of Liverpool, United Kingdom.
Anna SalernoInstitute of Integrative Biology, University of Liverpool, United Kingdom.
Theoni KatopodiInstitute of Integrative Biology, University of Liverpool, United Kingdom.
Rhys L WilliamsSchool of Cellular and Molecular Medicine, Faculty of Medical and Veterinary Sciences, University of Bristol, United Kingdom.
Christopher C WestThe University of Edinburgh, MRC Center for Regenerative Medicine, Scotland, United Kingdom.
Denis EvseenkoDepartment of Orthopaedic Surgery, University of Southern California (USC), Los Angeles, California, USA.
Ling WuDepartment of Orthopaedic Surgery, University of Southern California (USC), Los Angeles, California, USA.
Suzanna PangSchool of Cellular and Molecular Medicine, Faculty of Medical and Veterinary Sciences, University of Bristol, United Kingdom.
Roberta Ferro de GodoyRoyal National Orthopaedic Hospital, Institute of Orthopaedics and Musculoskeletal Science, University College London, Brockley Hill, Stanmore, United Kingdom.
Allen E GoodshipRoyal National Orthopaedic Hospital, Institute of Orthopaedics and Musculoskeletal Science, University College London, Brockley Hill, Stanmore, United Kingdom.
Bruno PéaultThe University of Edinburgh, MRC Center for Regenerative Medicine, Scotland, United Kingdom.
Ashley W BlomSchool of Clinical Sciences, Faculty of Medicine and Dentistry, University of Bristol, United Kingdom.
Wael KafienahSchool of Cellular and Molecular Medicine, Faculty of Medical and Veterinary Sciences, University of Bristol, United Kingdom.
Anthony P HollanderInstitute of Integrative Biology, University of Liverpool, United Kingdom.ORCID 0000-0003-2897-3747
University of Bristol · GBUniversity of Liverpool · GBRoyal National Orthopaedic Hospital · GBUniversity of Southern California · USMRC Centre for Regenerative Medicine · GBUniversity of California, Los Angeles · US

Funding

Chief Scientist Office CAF/11/13Medical Research Council G1000816Medical Research Council MR/K015648/1Medical Research Council MR/K015648/2
6 · The paper itself

Abstract

Multipotent mesenchymal stem cells (MSCs) have enormous potential in tissue engineering and regenerative medicine. However, until now, their development for clinical use has been severely limited as they are a mixed population of cells with varying capacities for lineage differentiation and tissue formation. Here, we identify receptor tyrosine kinase-like orphan receptor 2 (ROR2) as a cell surface marker expressed by those MSCs with an enhanced capacity for cartilage formation. We generated clonal human MSC populations with varying capacities for chondrogenesis. ROR2 was identified through screening for upregulated genes in the most chondrogenic clones. When isolated from uncloned populations, ROR2+ve MSCs were significantly more chondrogenic than either ROR2-ve or unfractionated MSCs. In a sheep cartilage-repair model, they produced significantly more defect filling with no loss of cartilage quality compared with controls. ROR2+ve MSCs/perivascular cells were present in developing human cartilage, adult bone marrow, and adipose tissue. Their frequency in bone marrow was significantly lower in patients with osteoarthritis (OA) than in controls. However, after isolation of these cells and their initial expansion in vitro, there was greater ROR2 expression in the population derived from OA patients compared with controls. Furthermore, osteoarthritis-derived MSCs were better able to form cartilage than MSCs from control patients in a tissue engineering assay. We conclude that MSCs expressing high levels of ROR2 provide a defined population capable of predictably enhanced cartilage production. Stem Cells 2017;35:2280-2291.

Indexed as

AnimalsCell DifferentiationCell ProliferationCells, CulturedChondrogenesisHumansMesenchymal Stem CellsReceptor Tyrosine Kinase-like Orphan ReceptorsSheepTissue EngineeringWnt-5a ProteinReceptor Tyrosine Kinase-like Orphan ReceptorsWnt-5a ProteinWNT5A protein, humanArthritisCell SignalingCellular therapyMesenchymal stem cellsTissue engineering

Identifiers

PMID28833807
PMCPMC5707440
OpenAlexW2756072256

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.