Evidence map›Paper›PMID 19664212›Full record

ArticleArthritis research & therapy2009

Treatment with ephrin B2 positively impacts the abnormal metabolism of human osteoarthritic chondrocytes.

Steeve Kwan Tat, Jean-Pierre Pelletier, Nathalie Amiable, Christelle Boileau, Martin Lavigne, Johanne Martel-Pelletier

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 32% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. A Novel EphA4 Signaling-Based Therapeutic Strategy for Osteoarthritis in Mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  4. Article
  5. Eph-Ephrin Signaling Mediates Cross-Talk Within the Bone Microenvironment.Frontiers in cell and developmental biology · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Icariin Alleviates Glucocorticoid-Induced Osteoporosis through EphB4/Ephrin-B2 Axis.Evidence-based complementary and alternative medicine : eCAM · 2020
    Article
  11. Role of IGF1 and EFN-EPH signaling in skeletal metabolism.Journal of molecular endocrinology · 2018
    Review
  12. Bidirectional ephrin signaling in bone.Osteoporosis and sarcopenia · 2016
    Review
  13. Article
  14. Article
  15. Membrane-mediated regulation of vascular identity.Birth defects research. Part C, Embryo today : reviews · 2016
    Review
  16. Article
  17. Early molecular responses of bone to estrogen deficiency induced by ovariectomy in rats.International journal of clinical and experimental medicine · 2015
    Article
  18. Ephrin B2/EphB4 mediates the actions of IGF-I signaling in regulating endochondral bone formation.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2014
    Article
  19. Targeting subchondral bone for treating osteoarthritis: what is the evidence?Best practice & research. Clinical rheumatology · 2010
    Review
  20. 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

6 authors at 3 institutions in 1 country.

Steeve Kwan TatOsteoarthritis Research Unit, University of Montreal Hospital Research Centre, Notre-Dame Hospital, 1560 Sherbrooke Street East, Montreal, Quebec, Canada. kwantats@yahoo.fr
Jean-Pierre Pelletier
Nathalie Amiable
Christelle Boileau
Martin Lavigne
Johanne Martel-Pelletier
Hôpital Notre-Dame · CAUniversité de Montréal · CAHôpital Maisonneuve-Rosemont · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMembers of the ephrin system, the ephrin receptor erythropoietin-producing hepatocellular B4 (EphB4) and its specific ligand, ephrin B2, appear to be involved in the bone remodelling process. We recently showed that their interaction inhibits the resorptive activity of human osteoarthritic (OA) subchondral bone osteoblasts. Hence, we further investigated the possible implication of these ephrin members on the catabolic/anabolic activities of human OA chondrocytes.

methodsEphB4 receptor and ephrin B2 levels were determined by quantitative PCR and immunohistochemistry, and the effects of ephrin B2 on the expression/production of factors involved in the OA process.

resultsEphB4 receptors and ephrin B2 ligands are expressed and produced by human normal and OA chondrocytes. Ephrin B2 protein was found at similar levels in both cartilage types, whereas EphB4 receptor expression (P < 0.0001) and production (P < 0.01) levels were significantly increased in OA chondrocytes/cartilage. Ephrin B2 treatment significantly inhibited the interleukin (IL)-1beta, IL-6, matrix metalloproteinase-1 (MMP-1), MMP-9, MMP-13, and proteinase-activated receptor-2 (PAR-2) gene expression levels, whereas MMP-2 was unaffected, and significantly increased collagen type II, a cartilage specific macromolecule. It also inhibited the IL-1beta stimulated protein production of IL-6, MMP-1 and MMP-13.

conclusionsOur study is the first to provide data on the presence and role of ephrin B2/EphB4 receptors in human chondrocytes/cartilage. Data showed that ephrin B2 treatment positively impacts the abnormal metabolism of OA cartilage by inhibiting important catabolic factors involved in this disease at the same time as increasing anabolic activity.

Indexed as

AgedCartilage, ArticularChondrocytesEnzyme-Linked Immunosorbent AssayEphrin-B2Gene ExpressionHumansImmunohistochemistryInterleukin-1betaInterleukin-6Matrix Metalloproteinase 1Matrix Metalloproteinase 13OsteoarthritisReceptor, EphB4Reverse Transcriptase Polymerase Chain ReactionEphrin-B2Interleukin-1betaInterleukin-6Matrix Metalloproteinase 1Matrix Metalloproteinase 13Receptor, EphB4

Identifiers

PMID19664212
PMCPMC2745802
OpenAlexW2058316664

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.