Comparison of the chondrosarcoma cell line SW1353 with primary human adult articular chondrocytes with regard to their gene expression profile and reactivity.

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Comparison of the chondrosarcoma cell line SW1353 with primary human adult articular chondrocytes with regard to their gene expression profile and reactivity to IL-1β  M. Gebauer, Ph.D., J. Saas, Ph.D., F. Sohler, M.Sc., J. Haag, M.Sc., S. Söder, M.D., M. Pieper, Ph.D., E. Bartnik, Ph.D., J. Beninga, Ph.D., R. Zimmer, Ph.D., T. Aigner, M.D., D.Sc.  Osteoarthritis and Cartilage  Volume 13, Issue 8, Pages 697-708 (August 2005) DOI: 10.1016/j.joca.2005.04.004 Copyright © 2005 OsteoArthritis Research Society International Terms and Conditions

Fig. 1 Two-dimensional hierarchical clustering of hybridization experiments from human SW1353 cells and PHCs stimulated in triplicate with 1ng/ml IL-1β at 30min, 6h, 16h, 24h and 48h. For the five time intervals of IL-1β stimulation, expression profiles of treated samples were compared to control samples (triplicates each). Dendrograms illustrate SW1353 expression values (a) and PHCs expression values (b) with genes that were significantly regulated by IL-1β in SW1353 cells (1.2× absolute fold-change and P-value<0.05 in at least two time points). Dendrograms (c) and (d) show the corresponding expression data for genes that were significantly regulated by IL-1β in PHCs (same criteria as above). Osteoarthritis and Cartilage 2005 13, 697-708DOI: (10.1016/j.joca.2005.04.004) Copyright © 2005 OsteoArthritis Research Society International Terms and Conditions

Fig. 2 Real-time PCR analysis of the IL-1β induced expression of IL-6 and LIF (a) and MMP-1, -3, and -13 (b) in SW1353 cells (solid bars) and PHCs (open bars) after 48h of stimulation with 1ng IL-1β (SW1353: three independent experiments; PHCs: six independent experiments). Osteoarthritis and Cartilage 2005 13, 697-708DOI: (10.1016/j.joca.2005.04.004) Copyright © 2005 OsteoArthritis Research Society International Terms and Conditions

Fig. 3 Representation of protease levels (a: MMP-1; b: MMP-3; c: MMP-13) secreted into the culture medium by SW1353 cells without and with stimulation by 0.1ng/ml IL-1β (for 24h). Total protease levels (i.e., active and pro-forms) were measured by the ELISA (given as ng/ml medium). Osteoarthritis and Cartilage 2005 13, 697-708DOI: (10.1016/j.joca.2005.04.004) Copyright © 2005 OsteoArthritis Research Society International Terms and Conditions

Fig. 4 Expression profiles of genes in the predicted NFκB regulation context (the only regulation context common to both systems according to our analysis) as log-ratios of expression levels between IL-1β stimulated cells and untreated cells against time in hours after the treatment. Profiles for SW1353 cells are shown as dashed lines, profiles for PHCs as solid lines. Correlation values quantify the similarity between the two systems for each gene. Statistical analysis showed that the correlation of the NFκB targets is significantly higher than expected by chance (details are given in the text). Osteoarthritis and Cartilage 2005 13, 697-708DOI: (10.1016/j.joca.2005.04.004) Copyright © 2005 OsteoArthritis Research Society International Terms and Conditions

Fig. 5 Expression profiles of genes in the predicted ATF2 regulation context as log-ratios of expression levels between IL-1β stimulated cells and untreated cells against time in hours after the treatment. Profiles for SW1353 cells are shown as dotted lines, profiles for PHCs as drawn lines. Correlation values quantify the similarity between the two systems for each gene. Statistical analysis showed that the correlation of the ATF2 targets is not significant (details are given in the text). (*The down-regulation of TNF-alpha after 16h in PHCs might represent a calculation error due to very low expression levels detected.) Osteoarthritis and Cartilage 2005 13, 697-708DOI: (10.1016/j.joca.2005.04.004) Copyright © 2005 OsteoArthritis Research Society International Terms and Conditions