Evidence map›Paper›PMID 23031212›Full record

ArticleArthritis research & therapy2012

Secretome analysis of chondroitin sulfate-treated chondrocytes reveals anti-angiogenic, anti-inflammatory and anti-catabolic properties.

Valentina Calamia, Lucía Lourido, Patricia Fernández-Puente, Jesús Mateos, Beatriz Rocha, Eulalia Montell, Josep Vergés, Cristina Ruiz-Romero, Francisco J Blanco

Open access · goldAbstract readComparative Study
In one paragraph

Article in Arthritis research & therapy, 2012. 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
3.2field-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, 58 citations in OpenAlex.

  1. Article
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  7. In Vitro Models and Proteomics in Osteoarthritis Research.Advances in experimental medicine and biology · 2023
    Review
  8. Cartilage Homeostasis and Osteoarthritis.International journal of molecular sciences · 2022
    Review
  9. Article
  10. Review
  11. Review
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  17. Development of an in vitro intervertebral disc innervation model to screen neuroinhibitory biomaterials.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2020
    Article
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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

9 authors at 4 institutions in 1 country.

Valentina Calamia
Lucía Lourido
Patricia Fernández-Puente
Jesús Mateos
Beatriz Rocha
Eulalia Montell
Josep Vergés
Cristina Ruiz-Romero
Francisco J Blanco
Instituto de Investigación Biomédica de A Coruña · ESBioibérica (Spain) · ESComplexo Hospitalario Universitario A Coruña · ESUniversidade da Coruña · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionChondroitin sulfate (CS) is a symptomatic slow-acting drug for osteoarthritis (OA) widely used in the clinic. The aim of this work is to find proteins whose secretion from cartilage cells under proinflammatory stimuli (IL-1β) is regulated by CS, employing a novel quantitative proteomic approach.

methodsHuman articular chondrocytes released from three normal cartilages were grown in SILAC medium. When complete incorporation of the heavy isotope was achieved, chondrocytes were stimulated with IL-1β 5 ng/ml with or without CS pretreatment (200 µg/ml). Forty-eight hours later, chondrocyte secretomes were analyzed by nano-scale liquid chromatography-mass spectrometry. Real-time PCR, western blot and immunohistochemistry analyses were employed to confirm some of the results.

resultsWe could identify 75 different proteins in the secretome of human articular chondrocytes. Eighteen of these were modulated by CS with statistical significance (six increased and 12 decreased). In normal chondrocytes stimulated with IL-1β, CS reduces inflammation directly by decreasing the presence of several complement components (CFAB, C1S, CO3, and C1R) and also indirectly by increasing proteins such as TNFα-induced protein (TSG6). TSG6 overexpression correlates with a decrease in pro-matrix metalloproteinase activation (observed in MMP1 and MMP3 levels). Finally, we observed a strong CS-dependent increase of an angiogenesis inhibitor, thrombospondin-1.

conclusionWe have generated a quantitative profile of chondrocyte extracellular protein changes driven by CS in the presence of IL-1β. We have also provided novel evidences of its anti-angiogenic, anti-inflammatory, and anti-catabolic properties. Demonstration of the anti-angiogenic action of CS might provide a novel therapeutic approach for OA targeting.

Indexed as

Anabolic AgentsAngiogenesis InhibitorsAnti-Inflammatory AgentsCell Adhesion MoleculesCells, CulturedChondrocytesChondroitin SulfatesComplement C1rComplement C1sHumansInterleukin-1betaMatrix Metalloproteinase 1Matrix Metalloproteinase 3Thrombospondin 1Anabolic AgentsAngiogenesis InhibitorsAnti-Inflammatory AgentsCell Adhesion MoleculesChondroitin SulfatesComplement C1rComplement C1sInterleukin-1betaMatrix Metalloproteinase 1Matrix Metalloproteinase 3Thrombospondin 1TNFAIP6 protein, human

Identifiers

PMID23031212
PMCPMC3580514
OpenAlexW2132980534

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.