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The samples were subsequently precipitated in 90% EtOH o/n, and next treated with dithioreitol (DTT) and iodoacetamide (IAA), followed by trypsination (1:50 trypsin:protein ratio). Peptides were analyzed by LC-MS on a Orbitrap Exploris mass spectrometer (Thermo Fisher Scientific), operated in the positive data-dependent acquisition (DDA) mode."],"repository":["Pride"],"quantification_method":[""],"modification":[""],"data_protocol":["Raw data was processed by Proteome Discoverer version 2.5 (Thermo Fisher Scientific) and peptides were identified using SEQUEST HT against UniProtKB human database (UP000005640_9606)."],"omics_type":["Proteomics"],"labhead":["Tobias Schmidt"],"instrument_platform":[""],"submission_type":["PARTIAL"],"labhead_affiliation":["Department of Pediatrics, Clinical Sciences Lund, Lund University, Lund, Sweden"],"species":["Homo Sapiens (human)"],"publication":["41761349 Schmidt T, Mossberg A, Król P, Kapetanovic MC, Einarsson JT, Croft AP, Bengtsson AA, Kahn F, Kahn R. Synovial fluid potentiates local fibroblasts to drive monocyte activation in juvenile idiopathic arthritis. Arthritis Res Ther. 2026 28(1):81 10.1186/s13075-026-03776-z"],"submitter_mail":["charlotte.welinder@med.lu.se"],"submitter_affiliation":["Dept. of Oncology, Clinical Sciences, Lund University, 221 85 Lund, Sweden"],"submitter_country":["Sweden"],"pubmed_abstract":["INTRODUCTION: Synovial fibroblasts (S-Fib) are recognized as key drivers of joint inflammation in adult arthritis. Moreover, data are limited on the processes driving monocyte activation in oligoarticular juvenile idiopathic arthritis (oJIA). Therefore, we aimed to explore if S-Fib from patients with oJIA induce monocyte activation. METHODS: S-Fib were isolated from the synovial fluid (SF) of n = 13 patients with oligoarticular juvenile idiopathic arthritis (oJIA) and n = 4 patients with rheumatoid arthritis (RA) to be used as a disease control. Healthy adult S-Fib were purchased. The interaction between monocytes and S-Fib was studied in co-cultures with monocytes isolated from healthy donors. These cells were analyzed by surface marker expression, cytokine production and T-cell activation. Moreover, S-Fib were “re-introduced” to the inflammatory synovial environment by priming or not with pooled cell-free SF from oJIA patients. The S-Fib were subsequently analyzed by cytokine production, ability to induce immune cell chemotaxis and mass spectrometry for proteomic changes, as well as their ability to induce monocyte activation as above. RESULTS: Co-culture with S-Fib induced inflammatory activation of healthy monocytes as characterized by increased CD86 and HLA-DR expression, cytokine production and subsequent T-cell activation. Importantly, there were only minor differences in monocyte activation pattern depending on the source of the co-cultured S-Fib (oJIA, RA or healthy). Interestingly, compared to S-Fib alone, priming of S-Fib with a pool of SF induced an inflammatory phenotype, production of IL-6 and enhanced chemotaxis of monocytes. Additionally, primed S-Fib induced a more pronounced inflammatory phenotype in healthy monocytes compared to S-Fib alone. Finally, direct cell-cell contact between S-Fib and monocytes was required for full induction of the observed monocyte activation. CONCLUSIONS: Our data show a contact dependent role for S-Fib in driving inflammation in oJIA by inducing pro-inflammatory monocytes, processes potentiated by inflamed SF. These data further support that targeting cell-cell interactions could be a viable option to explore for novel treatment strategies in arthritis."],"pubmed_title":["Synovial fluid potentiates local fibroblasts to drive monocyte activation in juvenile idiopathic arthritis."],"pubmed_authors":["Schmidt Tobias T, Mossberg Anki A, Król Petra P, Kapetanovic Meliha C MC, Einarsson Jon T JT, Croft Adam P AP, Bengtsson Anders A AA, Kahn Fredrik F, Kahn Robin R"],"additional_accession":[]},"is_claimable":false,"name":"Proteomic analysis of synovial fibroblasts from patients with Juvenile idiopathic arthritis","description":"The aim was to characterize the proteomic alterations in synovial fibroblasts from patients with juvenile idiopathic arthritis, with or without prior priming with inflamed synovial fluid. Synovial fibroblasts were isolated from the synovial fluid of patients with oligoarticular juvenile idiopathic arthritis via passaging. For the experiment, they were primed or not with a pool of 20% of pooled synovial fluid from patients for 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