A. Takahashi, M.C. de Andrés, K. Hashimoto, E. Itoi, R.O.C. Oreffo 

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Epigenetic regulation of interleukin-8, an inflammatory chemokine, in osteoarthritis  A. Takahashi, M.C. de Andrés, K. Hashimoto, E. Itoi, R.O.C. Oreffo  Osteoarthritis and Cartilage  Volume 23, Issue 11, Pages 1946-1954 (November 2015) DOI: 10.1016/j.joca.2015.02.168 Copyright © 2015 The Authors Terms and Conditions

Fig. 1 Diagrammatic representation of CpG sites within the proximal IL8 promoter with CpG sites and location of transcription factors indicated. Osteoarthritis and Cartilage 2015 23, 1946-1954DOI: (10.1016/j.joca.2015.02.168) Copyright © 2015 The Authors Terms and Conditions

Fig. 2 (A) Relative mRNA expression of IL8 in non-cultured primary human chondrocytes obtained from patients with femoral neck fracture (NOF) and OA patients. mRNA was analyzed by quantitative RT-PCR and normalized against GAPDH. (B) Percentage methylation of the indicated CpG sites in the IL8 proximal promoter in the same samples analysed by bisulfite pyrosequencing. Y-axis shows non-adjusted percentage methylation. Values are the mean ± SD of 15 independent samples from each group. **P < 0.01. Osteoarthritis and Cartilage 2015 23, 1946-1954DOI: (10.1016/j.joca.2015.02.168) Copyright © 2015 The Authors Terms and Conditions

Fig. 3 Results of Spearman's rank correlation coefficient comparing relative mRNA expression of IL8 and methylation status of the indicated CpG sites in the IL8 proximal promoter in OA chondrocytes (A) and controls (B). Osteoarthritis and Cartilage 2015 23, 1946-1954DOI: (10.1016/j.joca.2015.02.168) Copyright © 2015 The Authors Terms and Conditions

Fig. 4 Relative mRNA expression of IL8 was analyzed by quantitative RT-PCR and normalized against GAPDH in (A) pre-culture NOF chondrocytes and control culture chondrocytes, and (C) control culture and IL-1β culture. Percentage methylation of the indicated CpG sites in the IL8 proximal promoter was analysed using bisulfite pyrosequencing in (B) pre-culture NOF chondrocytes and control culture chondrocytes, and (D) control culture and IL-1β culture. Values are the mean ± SD of seven independent experiments. *P < 0.05, **P < 0.01. Osteoarthritis and Cartilage 2015 23, 1946-1954DOI: (10.1016/j.joca.2015.02.168) Copyright © 2015 The Authors Terms and Conditions

Fig. 5 IL8 promoter activity analysed by a luciferase assay in C28/I2 cell line transfected with non-methylated or methylated CpG-free vector containing wild-type IL8 promoter construct. (A) Basal activities without treatment. (B) Co-transfection with the empty control vector (pCMV4) or with the NF-κB p50 subunit expression vector, p65 subunit expression vector or both. (C) Co-transfection with the empty control vector (pcDNA3.1) or with the AP-1 c-Fos subunit expression vector, c-Jun subunit expression vector or both. (D) Co-transfection with the empty control vector (pcDNA3.1(+)) or with the C/EBPβ expression vector. Values are the mean ± SD of three independent experiments (B and C) or four (A and D). *P < 0.05, **P < 0.01. Osteoarthritis and Cartilage 2015 23, 1946-1954DOI: (10.1016/j.joca.2015.02.168) Copyright © 2015 The Authors Terms and Conditions

Fig. 6 Assessment of promoter activity of methylated or non-methylated IL8 promoter constructs containing different mutations analysed by luciferase assay. Point mutations (CG to TG) were created at CpG sites located at −31-bp, −106-bp, −116-bp, −116-bp and −106-bp, −116-bp and −31-bp, or −106-bp and −31-bp. (A) Basal IL8 promoter activity in C28/I2 cell line transfected with methylated or non-methylated CpG-free vector containing wild-type or mutated IL8 promoter constructs. (B) Co-transfection with the NF-κB p50 and p65 subunit expression vectors. (C) Co-transfection with the AP-1 c-Fos and c-Jun subunit expression vectors. (D) Co-transfection with the C/EBPβ expression vector. Values are the mean ± SD of three independent experiments. *P < 0.05, **P < 0.01. Osteoarthritis and Cartilage 2015 23, 1946-1954DOI: (10.1016/j.joca.2015.02.168) Copyright © 2015 The Authors Terms and Conditions