Mmendations and detected on Spectra Max 340PC (Molecular Devices). In the second experiment serum levels of Th1, Th2, Th17 and Th22 specific cytokines (IL-1a, IL-2, IL-4, IL-5, IL-6, IL-10, IL-13, IL-17A, IL21, IL-22, IL-27 and IFN-c) were measured using FlowCytomix Multiple Analyte Detection Mouse Th1/Th2/Th17/Th22 13plex Kit (eBioscience). The assay was run on FACSCanto IITM (BD Biosciences). Analyses were performed using FlowJo Software, Tree Star Inc. (Ashland, OR, USA).Fluorescence Activated Cell Sorting (FACS) Analyses and Cell CountingTo detect intracellular cytokine expression in different cell populations, a single cell preparation of lymph node and spleen was performed. The total number of cells in spleen was counted (Nucleocounter, ChemoMetec AS, Denmark). For FACS stainings, 16106 from lymph nodes or spleen 11967625 were placed in 96-well plates and pelleted (3 min, 300 g, 4uC). To avoid nonspecific binding via Fc-receptor interactions, cells were incubated with Fcblock (2.4G2, BD Biosciences, San Jose, CA, USA) for 10 min at room temperature. Antibodies used were anti-CD19 (clone ID3), anti-CD4 (clone RM4-5), anti-IL-10 (clone JES5-16E3) and antiIFN-c (clone XMG1.2) purchased from BD Biosciences, anti I-A/ I-E (clone M5/114.15.2 purchased from BioLegend, San Diego, CA, USA) and FoxP3 (clone FJK-16s), and IL-17 (clone eBio17B7), purchased from eBioscience (San Jose, CA, USA). ?All surface marker antibodies were diluted in FACS-buffer (PBS containing, 1 FCS and 0.5 mM EDTA). For intracellular staining with anti-IL-10 or isotype controls the cells wereDetermination of the Anti-CII-specific IgG AntibodiesFor 1480666 quantification of anti-CII antibodies in serum, 96-well plates (Nunc, Roskilde, Denmark) were coated overnight at 4uC with 10 mg/ml of native chicken CII (Sigma-Aldrich AB). The samples were serially diluted (1:250, 1:750, 1:2250, 1:6750) in 0.5 bovine serum albumin (BSA) (Sigma-Aldrich AB) in PBS. Biotinylated F(abN)2 fragments of goat anti-mouse IgG (Jackson Immuno Research Laboratories, Suffolk, England) were used as secondary antibody. Development was performed using horseradish peroxidase 0.5 mg/ml and 2.5 mg of the enzyme substrate 2,2azino-bis-(3-ethylbenzothiazoline sulfonic acid) (Sigma-Aldrich AB) per ml in citrate buffer (pH 4.2), containing 0.0075 H2O2. The absorbance was measured at 405 nm on Spectra Max 340PC (Molecular Devices, Sunnyvale, CA, USA).Disease-Dependent IL-10 MedChemExpress PS 1145 Ameliorates CIAStatistical AnalysisThe levels of IL-10 in supernatants after treatment with LNTGFP or LNT-IL-10 before and after LPS stimulation were compared using Two-way ANOVA (GraphPad Prism, GraphPad software, San Diego, CA, USA). All other statistical analysis between independent groups were calculated using the nonparametric Mann-Whitney U-test (GraphPad Prism) as described in the figure legends. A P-value #0.05 was regarded as being statistically significant.represents LNT-GFP and open circles and white bars LNT-IL-10 mice. (TIFF)Figure S2 Gating strategy for detecting IL-10 expression in CD19+MHCII+ B cells using flow cytometry. (TIFF)Vitamin D2 site AcknowledgmentsPrimer and probe sequences, and plasmid standards for real-time PCR quantification of the titin gene were kindly provided by Dr Anne Galy, Genethon, France. Plasmids pCMVDR8.74 and pMD.G2 were produced by Plasmid Factory, GmbH Co. KG, Bielefeld, Germany. We thank Anna-Carin Lundell for excellent statistical assistance and Professor IngaLill Martensson for invaluable help revising the manuscript.Mmendations and detected on Spectra Max 340PC (Molecular Devices). In the second experiment serum levels of Th1, Th2, Th17 and Th22 specific cytokines (IL-1a, IL-2, IL-4, IL-5, IL-6, IL-10, IL-13, IL-17A, IL21, IL-22, IL-27 and IFN-c) were measured using FlowCytomix Multiple Analyte Detection Mouse Th1/Th2/Th17/Th22 13plex Kit (eBioscience). The assay was run on FACSCanto IITM (BD Biosciences). Analyses were performed using FlowJo Software, Tree Star Inc. (Ashland, OR, USA).Fluorescence Activated Cell Sorting (FACS) Analyses and Cell CountingTo detect intracellular cytokine expression in different cell populations, a single cell preparation of lymph node and spleen was performed. The total number of cells in spleen was counted (Nucleocounter, ChemoMetec AS, Denmark). For FACS stainings, 16106 from lymph nodes or spleen 11967625 were placed in 96-well plates and pelleted (3 min, 300 g, 4uC). To avoid nonspecific binding via Fc-receptor interactions, cells were incubated with Fcblock (2.4G2, BD Biosciences, San Jose, CA, USA) for 10 min at room temperature. Antibodies used were anti-CD19 (clone ID3), anti-CD4 (clone RM4-5), anti-IL-10 (clone JES5-16E3) and antiIFN-c (clone XMG1.2) purchased from BD Biosciences, anti I-A/ I-E (clone M5/114.15.2 purchased from BioLegend, San Diego, CA, USA) and FoxP3 (clone FJK-16s), and IL-17 (clone eBio17B7), purchased from eBioscience (San Jose, CA, USA). ?All surface marker antibodies were diluted in FACS-buffer (PBS containing, 1 FCS and 0.5 mM EDTA). For intracellular staining with anti-IL-10 or isotype controls the cells wereDetermination of the Anti-CII-specific IgG AntibodiesFor 1480666 quantification of anti-CII antibodies in serum, 96-well plates (Nunc, Roskilde, Denmark) were coated overnight at 4uC with 10 mg/ml of native chicken CII (Sigma-Aldrich AB). The samples were serially diluted (1:250, 1:750, 1:2250, 1:6750) in 0.5 bovine serum albumin (BSA) (Sigma-Aldrich AB) in PBS. Biotinylated F(abN)2 fragments of goat anti-mouse IgG (Jackson Immuno Research Laboratories, Suffolk, England) were used as secondary antibody. Development was performed using horseradish peroxidase 0.5 mg/ml and 2.5 mg of the enzyme substrate 2,2azino-bis-(3-ethylbenzothiazoline sulfonic acid) (Sigma-Aldrich AB) per ml in citrate buffer (pH 4.2), containing 0.0075 H2O2. The absorbance was measured at 405 nm on Spectra Max 340PC (Molecular Devices, Sunnyvale, CA, USA).Disease-Dependent IL-10 Ameliorates CIAStatistical AnalysisThe levels of IL-10 in supernatants after treatment with LNTGFP or LNT-IL-10 before and after LPS stimulation were compared using Two-way ANOVA (GraphPad Prism, GraphPad software, San Diego, CA, USA). All other statistical analysis between independent groups were calculated using the nonparametric Mann-Whitney U-test (GraphPad Prism) as described in the figure legends. A P-value #0.05 was regarded as being statistically significant.represents LNT-GFP and open circles and white bars LNT-IL-10 mice. (TIFF)Figure S2 Gating strategy for detecting IL-10 expression in CD19+MHCII+ B cells using flow cytometry. (TIFF)AcknowledgmentsPrimer and probe sequences, and plasmid standards for real-time PCR quantification of the titin gene were kindly provided by Dr Anne Galy, Genethon, France. Plasmids pCMVDR8.74 and pMD.G2 were produced by Plasmid Factory, GmbH Co. KG, Bielefeld, Germany. We thank Anna-Carin Lundell for excellent statistical assistance and Professor IngaLill Martensson for invaluable help revising the manuscript.
