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Soluble syndecan-3 binds chemokines, reduces leukocyte migration in vitro and ameliorates disease severity in models of rheumatoid arthritis

Eustace, Andrew; McNaughton, EF; King, Sophie; Kehoe, Oksana; Kungl, Andreas; Mattey, Derek; Nobbs, AH; Williams, Neil; Middleton, Jim

Soluble syndecan-3 binds chemokines, reduces leukocyte migration in vitro and ameliorates disease severity in models of rheumatoid arthritis Thumbnail


Authors

Andrew Eustace

EF McNaughton

Sophie King

Andreas Kungl

Derek Mattey

AH Nobbs

Neil Williams

Jim Middleton



Abstract

Background
Syndecans are heparan sulfate proteoglycans that occur in membrane-bound or soluble forms. Syndecan-3, the least well-characterised of the syndecan family, is highly expressed on synovial endothelial cells in rheumatoid arthritis patients. Here, it binds pro-inflammatory chemokines with evidence for a role in chemokine presentation and leukocyte trafficking into the joint, promoting the inflammatory response. In this study, we explored the role of soluble syndecan-3 as a binder of chemokines and as an anti-inflammatory and therapeutic molecule.

Methods
A human monocytic cell line and CD14+ PBMCs were utilised in both Boyden chamber and trans-endothelial migration assays. Soluble syndecan-3 was tested in antigen-induced and collagen-induced in vivo arthritis models in mice. ELISA and isothermal fluorescence titration assays assessed the binding affinities. Syndecan-3 expression was identified by flow cytometry and PCR, and levels of shedding by ELISA.

Results
Using in vitro and in vivo models, soluble syndecan-3 inhibited leukocyte migration in vitro in response to CCL7 and its administration in murine models of rheumatoid arthritis reduced histological disease severity. Using isothermal fluorescence titration, the binding affinity of soluble syndecan-3 to inflammatory chemokines CCL2, CCL7 and CXCL8 was determined, revealing little difference, with Kds in the low nM range. TNFa increased cell surface expression and shedding of syndecan-3 from cultured human endothelial cells. Furthermore, soluble syndecan-3 occurred naturally in the sera of patients with rheumatoid arthritis and periodontitis, and its levels correlated with syndecan-1.

Conclusions
This study shows that the addition of soluble syndecan-3 may represent an alternative therapeutic approach in inflammatory disease.

Journal Article Type Article
Acceptance Date Jun 10, 2019
Publication Date Jul 12, 2019
Publicly Available Date Mar 29, 2024
Journal Arthritis Research & Therapy
Print ISSN 1478-6354
Publisher BioMed Central
Peer Reviewed Peer Reviewed
Volume 21
Article Number 172
DOI https://doi.org/10.1186/s13075-019-1939-2
Keywords Animal model, Cell migration, Chemokines, Syndecan-3, Therapeutic
Publisher URL https://arthritis-research.biomedcentral.com/articles/10.1186/s13075-019-1939-2#rightslink

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