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. 2024 Jul 31;44:36. doi: 10.1186/s41232-024-00347-0

Fig. 6.

Fig. 6

The effect of OSM and the JAK inhibitor on inflammatory and tissue-destructive properties of synovial fibroblasts. A Il6 and Tnfsf11 (RANKL) mRNA expression in mouse CIA synovial fibroblasts stimulated with indicated cytokines in the presence and absence of the JAK inhibitor (n = 3 per each condition). B Principal Components Analysis (PCA) plot of bulk mRNA sequencing of synovial fibroblasts in the three groups: untreated, OSM, OSM + JAKi treatments. C Heatmap of all significant gene expression. The genes which are significantly upregulated by OSM and then downregulated by the addition of the JAK inhibitor are marked in red. D Heatmap of selected inflammatory and tissue-destructive gene expression across the 3 groups. E mRNA expression of Il6, Cxcl1, Cxcl5, Tnfsf11, Mmp3 and Mmp13 across the 3 groups by qPCR analysis. F Gene Ontology (GO) Term Enrichment analysis using genes that were significant upregulated in OSM and downregulated by the addition of the JAK inhibitor (JAKi). Top 10 GO Terms are shown. G The JAK inhibitor inhibited osteoclastogenesis induced by CIA synovial fibroblasts under OSM stimulation. All data are expressed as the mean ± S.D. **p < 0.01, ***p < 0.001, ****p < 0.0001 by 1-way ANOVA with the Holm-Sidak multiple-comparison test (A, E and G), significant vs. all other groups (A and G)