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Elevated MSMP expression in FLSs and synovial tissues (STs) from patients with RA. A ‒ B <t>Microarray</t> sequencing revealed differentially expressed genes (DEGs) in FLSs from 5 RA patients and 5 healthy controls (HCs) by heatmap ( A ) and volcano diagram ( B ). |log2(fold change)|>1, false discovery rate (FDR) < 0.05. Orange, upregulated genes; blue, downregulated genes; grey, not significant genes. C MSMP mRNA expression was detected in a larger cohort of RA FLSs ( n = 38) and HCs ( n = 35) by RT-qPCR. FLSs samples were obtained from synovial cell bank established and maintained by our research team. D MSMP protein expression in RA FLSs ( n = 5) and HCs ( n = 5) was evaluated by Western blotting. Representative images are shown in the left panel. E The MSMP concentrations in the supernatants of RA FLSs ( n = 8) and HCs ( n = 8) were determined by ELISA. F ‒ G Co-expression of vimentin and MSMP in STs ( F ) and FLSs ( G ) from RA patients and HCs were detected by immunofluorescence. Representative images are shown. Red, vimentin; green, MSMP; blue, DAPI (nucleus). F Scale bar: 50 μm and 25 μm (red frame inset). G scale bar: 25 μm. H Serum MSMP concentration in HCs ( n = 62) and RA patients ( n = 65) were detected by ELISA. I The correlation of serum MSMP concentration from 65 RA patients with DAS28-ESR. Correlation analysis was performed by Spearman’s test. DAS28-ESR, disease activity score 28-erythrocyte sedimentation rate. The data are presented as the mean±SD. * P < 0.05 versus HC, by Student’s t test (for panels in C ‒ E and H )
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Elevated MSMP expression in FLSs and synovial tissues (STs) from patients with RA. A ‒ B <t>Microarray</t> sequencing revealed differentially expressed genes (DEGs) in FLSs from 5 RA patients and 5 healthy controls (HCs) by heatmap ( A ) and volcano diagram ( B ). |log2(fold change)|>1, false discovery rate (FDR) < 0.05. Orange, upregulated genes; blue, downregulated genes; grey, not significant genes. C MSMP mRNA expression was detected in a larger cohort of RA FLSs ( n = 38) and HCs ( n = 35) by RT-qPCR. FLSs samples were obtained from synovial cell bank established and maintained by our research team. D MSMP protein expression in RA FLSs ( n = 5) and HCs ( n = 5) was evaluated by Western blotting. Representative images are shown in the left panel. E The MSMP concentrations in the supernatants of RA FLSs ( n = 8) and HCs ( n = 8) were determined by ELISA. F ‒ G Co-expression of vimentin and MSMP in STs ( F ) and FLSs ( G ) from RA patients and HCs were detected by immunofluorescence. Representative images are shown. Red, vimentin; green, MSMP; blue, DAPI (nucleus). F Scale bar: 50 μm and 25 μm (red frame inset). G scale bar: 25 μm. H Serum MSMP concentration in HCs ( n = 62) and RA patients ( n = 65) were detected by ELISA. I The correlation of serum MSMP concentration from 65 RA patients with DAS28-ESR. Correlation analysis was performed by Spearman’s test. DAS28-ESR, disease activity score 28-erythrocyte sedimentation rate. The data are presented as the mean±SD. * P < 0.05 versus HC, by Student’s t test (for panels in C ‒ E and H )
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Elevated MSMP expression in FLSs and synovial tissues (STs) from patients with RA. A ‒ B <t>Microarray</t> sequencing revealed differentially expressed genes (DEGs) in FLSs from 5 RA patients and 5 healthy controls (HCs) by heatmap ( A ) and volcano diagram ( B ). |log2(fold change)|>1, false discovery rate (FDR) < 0.05. Orange, upregulated genes; blue, downregulated genes; grey, not significant genes. C MSMP mRNA expression was detected in a larger cohort of RA FLSs ( n = 38) and HCs ( n = 35) by RT-qPCR. FLSs samples were obtained from synovial cell bank established and maintained by our research team. D MSMP protein expression in RA FLSs ( n = 5) and HCs ( n = 5) was evaluated by Western blotting. Representative images are shown in the left panel. E The MSMP concentrations in the supernatants of RA FLSs ( n = 8) and HCs ( n = 8) were determined by ELISA. F ‒ G Co-expression of vimentin and MSMP in STs ( F ) and FLSs ( G ) from RA patients and HCs were detected by immunofluorescence. Representative images are shown. Red, vimentin; green, MSMP; blue, DAPI (nucleus). F Scale bar: 50 μm and 25 μm (red frame inset). G scale bar: 25 μm. H Serum MSMP concentration in HCs ( n = 62) and RA patients ( n = 65) were detected by ELISA. I The correlation of serum MSMP concentration from 65 RA patients with DAS28-ESR. Correlation analysis was performed by Spearman’s test. DAS28-ESR, disease activity score 28-erythrocyte sedimentation rate. The data are presented as the mean±SD. * P < 0.05 versus HC, by Student’s t test (for panels in C ‒ E and H )
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Elevated MSMP expression in FLSs and synovial tissues (STs) from patients with RA. A ‒ B Microarray sequencing revealed differentially expressed genes (DEGs) in FLSs from 5 RA patients and 5 healthy controls (HCs) by heatmap ( A ) and volcano diagram ( B ). |log2(fold change)|>1, false discovery rate (FDR) < 0.05. Orange, upregulated genes; blue, downregulated genes; grey, not significant genes. C MSMP mRNA expression was detected in a larger cohort of RA FLSs ( n = 38) and HCs ( n = 35) by RT-qPCR. FLSs samples were obtained from synovial cell bank established and maintained by our research team. D MSMP protein expression in RA FLSs ( n = 5) and HCs ( n = 5) was evaluated by Western blotting. Representative images are shown in the left panel. E The MSMP concentrations in the supernatants of RA FLSs ( n = 8) and HCs ( n = 8) were determined by ELISA. F ‒ G Co-expression of vimentin and MSMP in STs ( F ) and FLSs ( G ) from RA patients and HCs were detected by immunofluorescence. Representative images are shown. Red, vimentin; green, MSMP; blue, DAPI (nucleus). F Scale bar: 50 μm and 25 μm (red frame inset). G scale bar: 25 μm. H Serum MSMP concentration in HCs ( n = 62) and RA patients ( n = 65) were detected by ELISA. I The correlation of serum MSMP concentration from 65 RA patients with DAS28-ESR. Correlation analysis was performed by Spearman’s test. DAS28-ESR, disease activity score 28-erythrocyte sedimentation rate. The data are presented as the mean±SD. * P < 0.05 versus HC, by Student’s t test (for panels in C ‒ E and H )

Journal: Arthritis Research & Therapy

Article Title: MSMP promotes an aberrant phenotype of fibroblast-like synoviocytes in rheumatoid arthritis by blocking autophagy via the RUNX1/GPR137B axis

doi: 10.1186/s13075-026-03755-4

Figure Lengend Snippet: Elevated MSMP expression in FLSs and synovial tissues (STs) from patients with RA. A ‒ B Microarray sequencing revealed differentially expressed genes (DEGs) in FLSs from 5 RA patients and 5 healthy controls (HCs) by heatmap ( A ) and volcano diagram ( B ). |log2(fold change)|>1, false discovery rate (FDR) < 0.05. Orange, upregulated genes; blue, downregulated genes; grey, not significant genes. C MSMP mRNA expression was detected in a larger cohort of RA FLSs ( n = 38) and HCs ( n = 35) by RT-qPCR. FLSs samples were obtained from synovial cell bank established and maintained by our research team. D MSMP protein expression in RA FLSs ( n = 5) and HCs ( n = 5) was evaluated by Western blotting. Representative images are shown in the left panel. E The MSMP concentrations in the supernatants of RA FLSs ( n = 8) and HCs ( n = 8) were determined by ELISA. F ‒ G Co-expression of vimentin and MSMP in STs ( F ) and FLSs ( G ) from RA patients and HCs were detected by immunofluorescence. Representative images are shown. Red, vimentin; green, MSMP; blue, DAPI (nucleus). F Scale bar: 50 μm and 25 μm (red frame inset). G scale bar: 25 μm. H Serum MSMP concentration in HCs ( n = 62) and RA patients ( n = 65) were detected by ELISA. I The correlation of serum MSMP concentration from 65 RA patients with DAS28-ESR. Correlation analysis was performed by Spearman’s test. DAS28-ESR, disease activity score 28-erythrocyte sedimentation rate. The data are presented as the mean±SD. * P < 0.05 versus HC, by Student’s t test (for panels in C ‒ E and H )

Article Snippet: We obtained microarray data from the National Center for Biotechnology Information (NCBI) Gene Expression Omnibus (GEO) database ( GSE181614 ).

Techniques: Expressing, Microarray, Sequencing, Quantitative RT-PCR, Western Blot, Enzyme-linked Immunosorbent Assay, Immunofluorescence, Concentration Assay, Activity Assay, Sedimentation