Evidence map›Paper›PMID 26432574›Full record

ArticleInternational orthopaedics2015

The impact of hypoxia on mesenchymal progenitor cells of human skeletal tissue in the pathogenesis of heterotopic ossification.

Sebastian Winkler, Tanja Niedermair, Bernd Füchtmeier, Joachim Grifka, Susanne Grässel, Sven Anders, Guido Heers, Ferdinand Wagner

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In one paragraph

Article in International orthopaedics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  5. Neurovascular coupling in bone regeneration.Experimental & molecular medicine · 2022
    Review
  6. [Research progress of traumatic heterotopic ossification].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2022
    Review
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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 3 institutions in 1 country.

Sebastian WinklerDepartment of Orthopaedic Surgery, Regensburg University Medical Centre, Kaiser-Karl-V Allee 3, 93077, Bad Abbach, Germany. sebastianwinkler@email.de.
Tanja NiedermairDepartment of Orthopaedic Surgery, Regensburg University Medical Centre, Kaiser-Karl-V Allee 3, 93077, Bad Abbach, Germany. Tanja.Niedermair@klinik.uni-regensburg.de.
Bernd FüchtmeierDepartment of Orthopaedic Surgery and Traumatology, Hospital Barmherzige Brüder, Regensburg, Germany. Bernd.Fuechtmeier@barmherzige-regensburg.de.
Joachim GrifkaDepartment of Orthopaedic Surgery, Regensburg University Medical Centre, Kaiser-Karl-V Allee 3, 93077, Bad Abbach, Germany. Joachim.Grifka@ukr.de.
Susanne GrässelDepartment of Orthopaedic Surgery, Regensburg University Medical Centre, Kaiser-Karl-V Allee 3, 93077, Bad Abbach, Germany. Susanne.Graessel@klinik.uni-regensburg.de.
Sven AndersDepartment of Orthopaedic Surgery, Regensburg University Medical Centre, Kaiser-Karl-V Allee 3, 93077, Bad Abbach, Germany. Sven.Anders@ukr.de.
Guido HeersDepartment of Orthopaedic Surgery, Regensburg University Medical Centre, Kaiser-Karl-V Allee 3, 93077, Bad Abbach, Germany. Guido.Heers@ukr.de.
Ferdinand WagnerDepartment of Orthopaedic Surgery, Regensburg University Medical Centre, Kaiser-Karl-V Allee 3, 93077, Bad Abbach, Germany. Ferdinand.Wagner@ukr.de.
Asklepios Kliniken Bad Abbach · DEUniversity Hospital Regensburg · DEKrankenhaus Barmherzige Brüder · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMesenchymal progenitor cells (MPCs) are capable of differentiating into osteo/chondrogenic cells to contribute substantially to heterotopic ossification (HO). This study aimed to examine the impact of hypoxia on MPCs in the aetiology of HO.

methodsMPCs from human normal and HO skeletal tissue were cultivated under normoxia and hypoxia. Gene expression of factors which have a key role in HO aetiology (BMPs, COX-1 and COX-2, etc.) were examined by real-time PCR. Tissue of both groups was analysed by immunohistochemistry.

resultsUnder hypoxia, COX-1, -2 and SOX-9 gene expression was elevated in HO MPCs, whereas in normal muscle tissue only COX-2 was upregulated. MPCs from HO had a significantly elevated gene expression of BMP-4 and decreased expression of BMP-1 and HIF-1 under hypoxia compared to normal MPCs. Immunohistochemistry detected no significant differences between normal and HO tissue.

conclusionsHypoxia causes an enhanced gene expression of factors, which have a key role in HO pathophysiology. A better understanding of this entity will possibly allow reducing HO rates in orthopaedic and trauma surgery.

Indexed as

AdultAgedFemaleFlow CytometryGene ExpressionHumansHypoxiaImmunohistochemistryMaleMesenchymal Stem CellsMiddle AgedMuscle, SkeletalOssification, HeterotopicReal-Time Polymerase Chain ReactionYoung AdultHeterotopic ossificationHypoxiaMesenchymal progenitor cellPathogenesis

Identifiers

PMID26432574
OpenAlexW1910385849

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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.