Evidence map›Paper›PMID 26450135›Full record

ArticleStem cell research & therapy2015

Association between in vivo bone formation and ex vivo migratory capacity of human bone marrow stromal cells.

Rikke K Andersen, Walid Zaher, Kenneth H Larsen, Nicholas Ditzel, Katharina Drews, Wasco Wruck, James Adjaye, Basem M Abdallah, Moustapha Kassem

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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Identifying Biomarkers for Osteogenic Potency Assay Development.Advances in experimental medicine and biology · 2023
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  6. M2 Macrophages Promote PDGFRβFrontiers in pharmacology · 2021
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  11. Preparing Platelet-Rich Plasma with Whole Blood Harvested Intraoperatively During Spinal Fusion.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  12. Article
  13. Article
  14. 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

9 authors at 5 institutions in 4 countries.

Rikke K AndersenDepartment of Endocrinology and Metabolism, University Hospital of Odense, Odense, Denmark. rka@biomed.au.dk.
Walid ZaherDepartment of Endocrinology and Metabolism, University Hospital of Odense, Odense, Denmark. wzaher@health.sdu.dk.
Kenneth H LarsenDepartment of Endocrinology and Metabolism, University Hospital of Odense, Odense, Denmark. khaubergs@gmail.com.
Nicholas DitzelDepartment of Endocrinology and Metabolism, University Hospital of Odense, Odense, Denmark. nditzel@health.sdu.dk.
Katharina DrewsDepartment of Vertebrate Genomics, Molecular Embryology and Aging Group, Max Planck Institute for Molecular Genetics, Berlin, Germany. katharina_drews@gmx.de.
Wasco WruckResearch and Regenerative Medicine, Faculty of Medicine, Heinrich Heine University, Duesseldorf, Germany. Wasco.Wruck@med.uni-duesseldorf.de.
James AdjayeDepartment of Vertebrate Genomics, Molecular Embryology and Aging Group, Max Planck Institute for Molecular Genetics, Berlin, Germany. james.adjaye@med.uni-duesseldorf.de.
Basem M AbdallahDepartment of Endocrinology and Metabolism, University Hospital of Odense, Odense, Denmark. babdallah@health.sdu.dk.
Moustapha KassemDepartment of Endocrinology and Metabolism, University Hospital of Odense, Odense, Denmark. mkassem@health.sdu.dk.
Odense University Hospital · DKMax Planck Institute for Molecular Genetics · DEHeinrich Heine University Düsseldorf · DEHelwan University · EGUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThere is a clinical need for developing systemic transplantation protocols for use of human skeletal stem cells (also known bone marrow stromal stem cells) (hBMSC) in tissue regeneration. In systemic transplantation studies, only a limited number of hBMSC home to injured tissues suggesting that only a subpopulation of hBMSC possesses "homing" capacity. Thus, we tested the hypothesis that a subpopulation of hBMSC defined by ability to form heterotopic bone in vivo, is capable of homing to injured bone.

methodsWe tested ex vivo and in vivo homing capacity of a number of clonal cell populations derived from telomerized hBMSC (hBMSC-TERT) with variable ability to form heterotopic bone when implanted subcutaneously in immune deficient mice. In vitro transwell migration assay was used and the in vivo homing ability of transplanted hBMSC to bone fractures in mice was visualized by bioluminescence imaging (BLI). In order to identify the molecular phenotype associated with enhanced migration, we carried out comparative DNA microarray analysis of gene expression of hBMSC-derived high bone forming (HBF) clones versus low bone forming (LBF) clones.

resultsHBF clones were exhibited higher ex vivo transwell migration and following intravenous injection, better in vivo homing ability to bone fracture when compared to LBF clones. Comparative microarray analysis of HBF versus LBF clones identified enrichment of gene categories of chemo-attraction, adhesion and migration associated genes. Among these, platelet-derived growth factor receptor (PDGFR) α and β were highly expressed in HBF clones. Follow up studies showed that the chemoattractant effects of PDGF in vitro was more enhanced in HBF compared to LBF clones and this effect was reduced in presence of a PDGFRβ-specific inhibitor: SU-16 f. Also, PDGF exerted greater chemoattractant effect on PDGFRβ(+) cells sorted from LBF clones compared to PDGFRβ(-) cells.

conclusionOur data demonstrate phenotypic and molecular association between in vivo bone forming ability and migratory capacity of hBMSC. PDGFRβ can be used as a potential marker for the prospective selection of hBMSC populations with high migration and bone formation capacities suitable for clinical trials for enhancing bone regeneration.

Indexed as

Cell DifferentiationCell MovementAdipocytesAnimalsCells, CulturedHumansMesenchymal Stem CellsMice, Inbred NODMice, SCIDOsteogenesisReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor beta

Identifiers

PMID26450135
PMCPMC4599318
OpenAlexW1820629163

What OpenQuestion holds

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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.