Journalartikel

Disease-Specific Effects of Matrix and Growth Factors on Adhesion and Migration of Rheumatoid Synovial Fibroblasts


AutorenlisteLefevre, Stephanie; Schwarz, Maria; Meier, Florian M. P.; Zimmermann-Geller, Birgit; Tarner, Ingo H.; Rickert, Markus; Steinmeyer, Juergen; Sauerbier, Michael; Rehart, Stefan; Mueller-Ladner, Ulf; Neumann, Elena

Jahr der Veröffentlichung2017

Seiten4588-4595

ZeitschriftThe Journal of Immunology

Bandnummer198

Heftnummer12

ISSN0022-1767

eISSN1550-6606

DOI Linkhttps://doi.org/10.4049/jimmunol.1600989

VerlagAmerican Association of Immunologists


Abstract
In rheumatoid arthritis (RA), cartilage and bone matrix are degraded, and extracellular matrix (ECM) proteins, acting as cellular activators, are liberated. Similar to ECM proteins, matrix-bound chemokines, cytokines, and growth factors (GFs) influence functional properties of key cells in RA, especially synovial fibroblasts. The role of these molecules on attachment, migration, and proinflammatory and prodestructive activation of RASFs was analyzed. Adhesion/migration of RASFs were examined under GF-enriched (GF(+)) or -reduced (GF(-)) conditions with or without addition of matrix-associated GFs, TGF-beta, and plateletderived GF to GF 2 or culture supernatants. Fibroblast adhesion and alterations in proinflammatory/prodestructive properties (e.g., IL-6/matrix metalloproteinase 3-release) in response to matrix-associated molecules were compared. Effects of GF+, GF 2, and other ECM components on human RASF-mediated cartilage invasion were examined in the SCID mouse model. RASF adhesion under GF(-) conditions was significantly lower compared with GF(+) conditions (6.8-versus 8.3-fold). This effect was specific for RA because control cells showed opposite effects (e.g., osteoarthritis synovial fibroblasts [SF]; GF(-) versus GF+: 10.7-versus 8-fold). Addition of TGF-beta to GF(-) increased RASF attachment (12.7-fold) compared with other matrices and components. RASF adhesion to GF(+) matrix resulted in the strongest IL-6 and matrix metalloproteinase-3 release, and was even more pronounced compared with supplementation of single GFs. In vivo, GF(-) matrix decreased RASF-mediated cartilage invasion compared with GF(+) matrix. ECM components and especially GFs when bound within ECM actively enhance RASF attraction and cartilage adhesion. This observation was specific for RASFs as a reverse behavior was observed for controls.



Zitierstile

Harvard-ZitierstilLefevre, S., Schwarz, M., Meier, F., Zimmermann-Geller, B., Tarner, I., Rickert, M., et al. (2017) Disease-Specific Effects of Matrix and Growth Factors on Adhesion and Migration of Rheumatoid Synovial Fibroblasts, The Journal of Immunology, 198(12), pp. 4588-4595. https://doi.org/10.4049/jimmunol.1600989

APA-ZitierstilLefevre, S., Schwarz, M., Meier, F., Zimmermann-Geller, B., Tarner, I., Rickert, M., Steinmeyer, J., Sauerbier, M., Rehart, S., Mueller-Ladner, U., & Neumann, E. (2017). Disease-Specific Effects of Matrix and Growth Factors on Adhesion and Migration of Rheumatoid Synovial Fibroblasts. The Journal of Immunology. 198(12), 4588-4595. https://doi.org/10.4049/jimmunol.1600989



Schlagwörter


FACTOR-BETAinflammatory arthritisINTEGRIN RECEPTORSKAPPA-BMETALLOPROTEINASE PRODUCTIONSYNOVIOCYTES


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