Evidence map›Paper›PMID 18975308›Full record

ArticleArthritis and rheumatism2008

Inhibition of interleukin-1beta-induced matrix metalloproteinases 1 and 13 production in human osteoarthritic chondrocytes by prostaglandin D2.

Nadia Zayed, Hassan Afif, Nadir Chabane, Leandra Mfuna-Endam, Mohamed Benderdour, Johanne Martel-Pelletier, Jean-Pierre Pelletier, Rajender K Motiani, Mohamed Trebak, Nicolas Duval and 1 more

Open access · greenAbstract read
In one paragraph

Article in Arthritis and rheumatism, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.7field-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

29 citing papers in PubMed, 59 citations in OpenAlex.

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  17. Persisting eicosanoid pathways in rheumatic diseases.Nature reviews. Rheumatology · 2014
    Review
  18. Article
  19. Review
  20. Neuronal prostaglandin E2 receptor subtype EP3 mediates antinociception during inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2013
    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

11 authors at 3 institutions in 2 countries.

Nadia ZayedCentre Hospitalier de l'Université de Montréal, Notre Dame Hospital, and University of Montreal, Montreal, Quebec, Canada.
Hassan Afif
Nadir Chabane
Leandra Mfuna-Endam
Mohamed Benderdour
Johanne Martel-Pelletier
Jean-Pierre Pelletier
Rajender K Motiani
Mohamed Trebak
Nicolas Duval
Hassan Fahmi
Université de Montréal · CAAlbany Medical Center Hospital · USHôpital du Sacré-Cœur de Montréal · CA

Funding

Role of calcium and reactive oxygen species in toxicant-induced immune failureK22ES014729 · NIEHS · ALBANY MEDICAL COLLEGE · PI TREBAK, MOHAMED · 2007 to 2009
$448k
NIEHS NIH HHS K22 ES014729NIEHS NIH HHS K22-ES-014729
6 · The paper itself

Abstract

objectiveTo investigate the effects of prostaglandin D2 (PGD2) on interleukin-1beta (IL-1beta)-induced matrix metalloproteinase 1 (MMP-1) and MMP-13 expression in human chondrocytes and the signaling pathways involved in these effects.

methodsChondrocytes were stimulated with IL-1 in the presence or absence of PGD2, and expression of MMP-1 and MMP-13 proteins was evaluated by enzyme-linked immunosorbent assay. Messenger RNA (mRNA) expression and promoter activity were analyzed by real-time reverse transcription-polymerase chain reaction and transient transfections, respectively. The role of the PGD2 receptors D prostanoid receptor 1 (DP1) and chemoattractant receptor-like molecule expressed on Th2 cells (CRTH2) was evaluated using specific agonists and antibody-blocking experiments. The contribution of the cAMP/protein kinase A (PKA) pathway was determined using cAMP-elevating agents and PKA inhibitors.

resultsPGD2 decreased in a dose-dependent manner IL-1-induced MMP-1 and MMP-13 protein and mRNA expression as well as their promoter activation. DP1 and CRTH2 were expressed and functional in chondrocytes. The effect of PGD2 was mimicked by BW245C, a selective agonist of DP1, but not by 13,14-dihydro-15-keto-PGD2, a selective agonist of CRTH2. Furthermore, treatment with an anti-DP1 antibody reversed the effect of PGD2, indicating that the inhibitory effect of PGD2 is mediated by DP1. The cAMP-elevating agents 8-Br-cAMP and forskolin suppressed IL-1-induced MMP-1 and MMP-13 expression, and the PKA inhibitors KT5720 and H89 reversed the inhibitory effect of PGD2, suggesting that the effect of PGD2 is mediated by the cAMP/PKA pathway.

conclusionPGD2 inhibits IL-1-induced production of MMP-1 and MMP-13 by chondrocytes through the DP1/cAMP/PKA signaling pathway. These data also suggest that modulation of PGD2 levels in the joint may have therapeutic potential in the prevention of cartilage degradation.

Indexed as

8-Bromo Cyclic Adenosine MonophosphateAgedAntibodiesCarbazolesCells, CulturedChondrocytesColforsinCyclic AMPCyclic AMP-Dependent Protein KinasesEnzyme-Linked Immunosorbent AssayHumansInterleukin-1betaIsoquinolinesMatrix Metalloproteinase 1Matrix Metalloproteinase 13Osteoarthritis13,14-dihydro-15-ketoprostaglandin D28-Bromo Cyclic Adenosine MonophosphateAntibodiesCarbazolesColforsinCyclic AMPCyclic AMP-Dependent Protein KinasesInterleukin-1betaIsoquinolinesKT 5720LTB4R protein, humanMatrix Metalloproteinase 1Matrix Metalloproteinase 13N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamideProstaglandin D2prostaglandin D2 receptorprostanoid D receptor 1, humanPyrrolesReceptors, ImmunologicReceptors, Leukotriene B4Receptors, ProstaglandinRNA, MessengerSulfonamides

Identifiers

PMID18975308
PMCPMC2657141
OpenAlexW1978025097

What OpenQuestion holds

Textmetadata
LicenceTDM
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.