Evidence map›Paper›PMID 12000725›Full record

ArticleThe American journal of pathology2002

Adenoviral transfer of murine oncostatin M elicits periosteal bone apposition in knee joints of mice, despite synovial inflammation and up-regulated expression of interleukin-6 and receptor activator of nuclear factor-kappa B ligand.

Alfons S K de Hooge, Fons A J van de Loo, Miranda B Bennink, Diana S de Jong, Onno J Arntz, Erik Lubberts, Carl D Richards, Wim B vandDen Berg

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

22 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. A roadmap to target interleukin-6 in osteoarthritis.Rheumatology (Oxford, England) · 2020
    Article
  7. Impact of Bacterial Infections on Osteogenesis: Evidence From In Vivo Studies.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2019
    Review
  8. Macrophages and skeletal health.Pharmacology & therapeutics · 2017
    Review
  9. Article
  10. Article
  11. Macrophage Polarization and Bone Formation: A review.Clinical reviews in allergy & immunology · 2016
    Review
  12. Article
  13. Fuzzy clustering analysis of osteosarcoma related genes.Pathology oncology research : POR · 2014
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  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

8 authors at 4 institutions in 3 countries.

Alfons S K de HoogeRheumatology Research Laboratory, University Medical Center Nijmegen, Nijmegen, The Netherlands. a.dehooge@reuma.azn.nl
Fons A J van de Loo
Miranda B Bennink
Diana S de Jong
Onno J Arntz
Erik Lubberts
Carl D Richards
Wim B vandDen Berg
Radboud University Medical Center · NLRadboud University Nijmegen · NLCatholic University of America · USMcMaster University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncostatin M (OSM) has been described as a bone-remodeling factor either stimulating osteoblast activity or osteoclast formation in vitro. To elucidate the in vivo effect of OSM on bone remodeling, we injected an adenoviral vector encoding murine OSM in knee joints of mice. OSM strongly induced interleukin (IL)-6 gene expression, a known mediator of osteoclast development. We investigated the OSM effect in wild-type and IL-6-deficient mice and found a similar degree of OSM-induced joint inflammation. Within the first week of inflammation, the periosteum along the femur and tibia increased in cell number and stained positive for the osteoblast marker alkaline phosphatase. At these sites bone apposition occurred in both strains as demonstrated by Goldner and Von Kossa staining. In vitro OSM enhanced the effect of bone morphogenetic protein-2 on osteoblast differentiation. Immunohistochemistry demonstrated expression of receptor activator of nuclear factor-kappa B ligand (RANKL) and its receptor, receptor activator of nuclear factor-kappa B (RANK), in the periosteum but osteoclasts were not detected at sites of bone apposition. Induced mRNA expression for the receptor activator of nuclear factor-kappa B ligand inhibitor osteoprotegerin probably controlled osteoclast development during OSM overexpression. Our results show that OSM favors bone apposition at periosteal sites instead of resorption in vivo. This effect was not dependent on or inhibited by IL-6.

Indexed as

Transforming Growth Factor betaAdenoviridaeAlkaline PhosphataseAnimalsArthritisBone Morphogenetic Protein 2Bone Morphogenetic ProteinsCarrier ProteinsCell LineDose-Response Relationship, DrugGene ExpressionGene Transfer TechniquesGenotypeGlycoproteinsInterleukin-6Knee JointAlkaline PhosphataseBmp2 protein, mouseBone Morphogenetic Protein 2Bone Morphogenetic ProteinsCarrier ProteinsGlycoproteinsInterleukin-6Membrane GlycoproteinsOncostatin MOsm protein, mouseOsteoprotegerinPeptidesRANK LigandReceptor Activator of Nuclear Factor-kappa BReceptors, Cytoplasmic and NuclearReceptors, Tumor Necrosis FactorRecombinant ProteinsTnfrsf11a protein, mouseTnfrsf11b protein, mouseTnfsf11 protein, mouseTransforming Growth Factor beta

Identifiers

PMID12000725
PMCPMC1850853
OpenAlexW2014057800

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.