Evidence map›Paper›PMID 19264156›Full record

ArticleBone2009

Proteinase-activated receptor (PAR)-2 activation impacts bone resorptive properties of human osteoarthritic subchondral bone osteoblasts.

Nathalie Amiable, Steeve Kwan Tat, Daniel Lajeunesse, Nicolas Duval, Jean-Pierre Pelletier, Johanne Martel-Pelletier, Christelle Boileau

Open access · greenAbstract read
In one paragraph

Article in Bone, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Protease Activated Receptors and Arthritis.International journal of molecular sciences · 2021
    Review
  7. Article
  8. [Research progress on protease-activated receptor 2 in pathogenesis of osteoarthritis].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2017
    Review
  9. Review
  10. Review
  11. Evaluation of antibodies directed against human protease-activated receptor-2.Naunyn-Schmiedeberg's archives of pharmacology · 2012
    Article
  12. Article
  13. Review
  14. Article
  15. The bone-cartilage unit in osteoarthritis.Nature reviews. Rheumatology · 2011
    Review
  16. 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

7 authors at 2 institutions in 1 country.

Nathalie AmiableOsteoarthritis Research Unit, University of Montreal Hospital Centre (CRCHUM), Notre-Dame Hospital, 1560 Sherbrooke Street East, Montreal, Quebec, Canada. amiablenathalie@hotmail.com
Steeve Kwan Tat
Daniel Lajeunesse
Nicolas Duval
Jean-Pierre Pelletier
Johanne Martel-Pelletier
Christelle Boileau
Hôpital Notre-Dame · CAUniversité de Montréal · CA

Funding

CIHR 49501
6 · The paper itself

Abstract

introductionIn osteoarthritis (OA), the subchondral bone undergoes a remodelling process involving several factors synthesized by osteoblasts. In this study, we investigated the expression, production, modulation, and role of PAR-2 in human OA subchondral bone osteoblasts. MATERIALS AND

methodsPAR-2 expression and production were determined by real-time PCR and flow cytometry, respectively. PAR-2 modulation was investigated in OA subchondral bone osteoblasts treated with IL-1 beta (100 pg/ml), TNF-alpha (5 ng/ml), TGF-beta1 (10 ng/ml), PGE(2) (500 nM), IL-6 (10 ng/ml) and IL-17 (10 ng/ml). Membranous RANKL protein was assessed by flow cytometry, and OPG, MMP-1, MMP-9, MMP-13, IL-6 and intracellular signalling pathways by specific ELISAs. Bone resorptive activity was measured by using a co-culture model of human PBMC and OA subchondral bone osteoblasts.

resultsPAR-2 expression and production (p<0.05) were markedly increased when human OA subchondral bone osteoblasts were compared to normal. On OA osteoblasts, PAR-2 production was significantly increased by IL-1 beta, TNF-alpha and PGE(2). Activation of PAR-2 with a specific agonist, SLIGKV-NH(2), induced a significant up-regulation of MMP-1, MMP-9, IL-6, and membranous RANKL, but had no effect on MMP-13 or OPG production. Interestingly, bone resorptive activity was also significantly enhanced following PAR-2 activation. The PAR-2 effect was mediated by activation of the MAP kinases Erk1/2 and JNK.

conclusionThis study is the first to demonstrate that PAR-2 activation plays a role in OA subchondral bone resorption via an up-regulation of major bone remodelling factors. These results shed new light on the potential of PAR-2 as a therapeutic target in OA.

Indexed as

AgedAged, 80 and overBone ResorptionCells, CulturedDinoprostoneEnzyme-Linked Immunosorbent AssayFlow CytometryHumansInterleukin-17Interleukin-1betaInterleukin-6Matrix Metalloproteinase 1Matrix Metalloproteinase 13Matrix Metalloproteinase 9Middle AgedOsteoarthritisDinoprostoneInterleukin-17Interleukin-1betaInterleukin-6Matrix Metalloproteinase 1Matrix Metalloproteinase 13Matrix Metalloproteinase 9RANK LigandReceptor, PAR-2Transforming Growth Factor beta1Tumor Necrosis Factor-alpha

Identifiers

PMID19264156
PMCPMC5250314
OpenAlexW2163147493

What OpenQuestion holds

Textmetadata
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.