Evidence map›Paper›PMID 42019906›Full record

ArticleOsteoarthritis and cartilage2026

Osteoarthritic synovial fibroblasts drive inflammatory responses and impair chondrocyte function in response to a fibronectin matrikine.

Jorge G Fernandez Davila, Ralph A Alberto, Seyoun Byun, Susan D'Costa, Jacqueline Shine, Carolina Alvarez, Adam B Yanke, Christopher W Olcott, Brian O Diekman, Douglas H Phanstiel and 1 more

Abstract read
In one paragraph

Article in Osteoarthritis and cartilage, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Jorge G Fernandez DavilaThurston Arthritis Research Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA. Electronic address: jfernan@email.unc.edu.
Ralph A AlbertoThurston Arthritis Research Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA. Electronic address: ra3108@cumc.columbia.edu.
Seyoun ByunCurriculum in Bioinformatics and Computational Biology, University of North Carolina, Chapel Hill, NC, USA. Electronic address: sbyun@unc.edu.
Susan D'CostaThurston Arthritis Research Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA. Electronic address: susan_dcosta@med.unc.edu.
Jacqueline ShineThurston Arthritis Research Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA. Electronic address: yalins@med.unc.edu.
Carolina AlvarezThurston Arthritis Research Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA. Electronic address: alvarec@emaill.edu.
Adam B YankeDepartment of Orthopedics, Rush University Medical Center, Chicago, IL, USA. Electronic address: adam.yanke@rushortho.com.
Christopher W OlcottThurston Arthritis Research Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA; Department of Orthopedics, University of North Carolina School of Medicine, Chapel Hill, NC, USA. Electronic address: chistopher_olcott@med.unc.edu.
Brian O DiekmanThurston Arthritis Research Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA; Lampe Joint Department of Biomedical Engineering, University of North Carolina and North Carolina State University, Raleigh, NC, USA. Electronic address: bdiekman@email.unc.edu.
Douglas H PhanstielThurston Arthritis Research Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA; Curriculum in Bioinformatics and Computational Biology, University of North Carolina, Chapel Hill, NC, USA; Department of Cell Biology and Physiology, University of North Carolina School of Medicine, Chapel Hill, NC, USA. Electronic address: douglas_phanstiel@med.unc.edu.
Richard F LoeserThurston Arthritis Research Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA; Division of Rheumatology, Allergy and Immunology, University of North Carolina School of Medicine, Chapel Hill, NC, USA. Electronic address: richard_loeser@med.unc.edu.

Funding

Identifying novel osteoarthritis risk genes using GWAS, chondrocyte genomics, and genome editingR01AR079538 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RICHARD F LOESER, Douglas H. Phanstiel · 2022 to 2026
$2.4M
Predoctoral Training Program in Bioinformatics and Computational BiologyT32GM135123 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Michael Isaiah Love, William Valdar · 2021 to 2026
$1.7M
The effect of genetic variation on mRNA splicing in chondrocytes responding to cartilage matrix damageF31AR083722 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SEYOUN BYUN · 2024 to 2026
$124k
NIAMS NIH HHS F31 AR083722NIAMS NIH HHS R01 AR079538NIGMS NIH HHS T32 GM135123
6 · The paper itself

Abstract

objectiveTo investigate the effects of a matrikine, fibronectin fragment (FN7-10), on human osteoarthritic (OA) synovial fibroblasts and implications for inflammation and cartilage degradation.

designJoint tissue was obtained from 50 OA patients undergoing knee arthroplasty. Isolated synovial fibroblasts were treated with 1 µM of FN7-10 or PBS as control. Cytokine protein arrays were used to identify differentially secreted inflammatory mediators in conditioned media (CM). Bulk RNA-seq was used to evaluate transcriptional changes. Monocytic THP-1 cells in transwell assays were used to evaluate chemotactic activity of CM. Macrophage differentiation of THP-1 cells was assessed via qPCR and flow cytometry. Chondrocyte gene expression was evaluated by qPCR and glycosaminoglycan (GAG) production by Alcian blue assays.

resultsFN7-10 stimulation of synovial fibroblasts induced an inflammatory secretome, including production of chemokines. RNA-seq analysis confirmed FN7-10 induced upregulation of chemokines, including CCL5, CCL7, CCL8, CCL20, CXCL5 and CXCL10, which displayed mean transcriptional log-2-fold changes of 3.89 (CI, 2.81 - 4.97). CM from FN7-10-stimulated synovial fibroblasts increased THP-1 chemotaxis by 7.8-fold (CI, 3.26 - 12.35) which was reduced by CCR2 or CXCR2 inhibitors and promoted monocyte to macrophage differentiation characterized by an increase in pro-inflammatory gene expression and CD14. Chondrocytes treated with FN7-10 synovial fibroblast CM showed elevated IL6 and MMP1 and decreased ACAN and COL2A1 expression, along with reduced GAG levels.

conclusionsThe matrikine FN7-10 promotes an inflammatory synovial fibroblast phenotype. Proinflammatory mediators, including chemokines, released from activated synovial fibroblasts recruit monocytes that may exacerbate joint inflammation and can also promote increased catabolic activity in chondrocytes.

Indexed as

ChondrocytesFibroblastsFibronectinsOsteoarthritis, KneeSynovial MembraneCell DifferentiationCells, CulturedChemokinesCytokinesFemaleHumansInflammationTHP-1 CellsChemokinesCytokinesFibronectinsCell-cell communicationFibronectin-FragmentInflammationOsteoarthritisSynovial Fibroblasts

Identifiers

PMID42019906
PMCPMC13158885

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.