Evidence map›Paper›PMID 32586320›Full record

ArticleBMC molecular and cell biology2020

Alterations in the chondrocyte surfaceome in response to pro-inflammatory cytokines.

Bernadette Jeremiasse, Csaba Matta, Christopher R Fellows, David J Boocock, Julia R Smith, Susan Liddell, Floris Lafeber, Willem E van Spil, Ali Mobasheri

Abstract read
In one paragraph

Article in BMC molecular and cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Pro-resolving Annexin A1-derived peptide Ac2-26 reduces nociception and mitigates joint damage in experimental osteoarthritis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  2. Article
  3. Article
  4. Introduction: Methods for Studying the Plasma Membrane and the Surfaceome.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  5. Article
  6. Article
  7. CaInternational journal of molecular sciences · 2023
    Review
  8. Review
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  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Experimental Therapeutics for the Treatment of Osteoarthritis.Journal of experimental pharmacology · 2021
    Review
  17. Journal of proteome research · 2020
    Article
  18. 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

9 authors.

Bernadette JeremiasseDepartment of Rheumatology & Clinical Immunology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Csaba MattaDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary. matta.csaba@med.unideb.hu.ORCID http://orcid.org/0000-0002-9678-7420
Christopher R FellowsDepartment of Veterinary Pre-Clinical Sciences, School of Veterinary Science and Medicine, University of Surrey, Guildford, UK.
David J BoocockJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham, NG11 8NS, UK.
Julia R SmithBruker UK Limited, Coventry, UK.
Susan LiddellExonate Ltd., Medicity, Thane Road, Nottingham, UK.
Floris LafeberDepartment of Rheumatology & Clinical Immunology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Willem E van SpilDepartment of Rheumatology & Clinical Immunology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Ali MobasheriDepartment of Rheumatology & Clinical Immunology, University Medical Centre Utrecht, Utrecht, The Netherlands. ali.mobasheri@oulu.fi.ORCID http://orcid.org/0000-0001-6261-1286

Funding

Arthritis Research UK 20194European Social Fund DOTSUT-215FP7 People: Marie-Curie Actions 625746Seventh Framework Programme HEALTH.2012.2.4.5-2
6 · The paper itself

Abstract

backgroundChondrocytes are exposed to an inflammatory micro-environment in the extracellular matrix (ECM) of articular cartilage in joint diseases such as osteoarthritis (OA) and rheumatoid arthritis (RA). In OA, degenerative changes and low-grade inflammation within the joint transform the behaviour and metabolism of chondrocytes, disturb the balance between ECM synthesis and degradation, and alter the osmolality and ionic composition of the micro-environment. We hypothesize that chondrocytes adjust their physiology to the inflammatory microenvironment by modulating the expression of cell surface proteins, collectively referred to as the 'surfaceome'. Therefore, the aim of this study was to characterize the surfaceome of primary equine chondrocytes isolated from healthy joints following exposure to the pro-inflammatory cytokines interleukin-1-beta (IL-1β) and tumour necrosis factor-alpha (TNF-α). We employed combined methodology that we recently developed for investigating the surfaceome in stem cells. Membrane proteins were isolated using an aminooxy-biotinylation technique and analysed by mass spectrometry using high throughput shotgun proteomics. Selected proteins were validated by western blotting.

resultsAmongst the 431 unique cell surface proteins identified, a high percentage of low-abundance proteins, such as ion channels, receptors and transporter molecules were detected. Data are available via ProteomeXchange with identifier PXD014773. A high number of proteins exhibited different expression patterns following chondrocyte stimulation with pro-inflammatory cytokines. Low density lipoprotein related protein 1 (LPR-1), thrombospondin-1 (TSP-1), voltage dependent anion channel (VDAC) 1-2 and annexin A1 were considered to be of special interest and were analysed further by western blotting.

conclusionsOur results provide, for the first time, a repository for proteomic data on differentially expressed low-abundance membrane proteins on the surface of chondrocytes in response to pro-inflammatory stimuli.

Indexed as

AnimalsBiomarkersCartilage, ArticularCells, CulturedChondrocytesCytokinesHorsesInflammationInterleukin-1betaMass SpectrometryMembrane ProteinsOsteoarthritisPrimary Cell CultureProteomicsTumor Necrosis Factor-alphaBiomarkersCytokinesInterleukin-1betaMembrane ProteinsTumor Necrosis Factor-alphaAminooxy-biotinBiomarkerChondrocyteInflammationMass spectrometryOsteoarthritisProteomicsSurfaceome

Identifiers

PMID32586320
PMCPMC7318434

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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.