Er panel) or a cytokine combination (10 ng/ml IL-1b+10 ng

Er panel) or a cytokine combination (10 ng/ml IL-1b+10 ng/ml IFN-c, middle and lower panel). Western blot analyses were performed for full length and cleaved caspase-3 (upper panel), phospho-NF-kB p65 (Ser536) and NF-kB p65 (middle panel) and phospho-p53 (Ser15) (lower panel). GAPDH or beta-actin were used as loading control. All panels show one typical blot out of three independent experiments. *p,0.05 compared to untreated control. doi:10.1371/journal.pone.0054106.gMeasurement of Intracellular NAD LevelThe get Conduritol B epoxide concentrations of NAD in the whole cell extracts were analysed by a commercially available NAD/NADH assay kit ?(EnzyChromTM NAD/NADH Assay Kit; Koln, Germany). Therefore, 500,000 cells/well were seeded in 6well plates and cultured as described above. After treatment for 2 or 48 h, cells were trypsinized and 2 wells per sample were pooled and lysed in 100 ml NAD extraction buffer. To homogenize the samples, cell extracts were undergo freeze/thaw cycles. NAD level were determined according to manufacturer’s instructions. The cell pellet of each sample was resuspended in 100 ml 2 SDS, shaked for 10 min at 99uC and centrifuged for 5 min at 20,0006g and then used for protein determination (BCA Assay, Pierce Thermo Scientific). The NAD level of each sample was referred to the corresponding total protein amount of the sample.Western BlottingINS-1E cells were seeded into 6well plates at 500,000 cells/w ell and grown in buy CX-4945 culture medium. After 72 h, cells were incubated in serum free medium for 24 h. Thereafter, cells were incubated for 48 h for activated caspase-3, 6 h for p53 and 3 h for NF-kB detection under serum free conditions in the absence or presence of the treatment conditions. Equal amounts of protein from each treatment group were run on 10 or 15 SDS olyacrylamide gels. After semi-dry transfer onto nitrocellulose, membranes (0.45 mm) were blocked and subsequently incubated with rabbit anti-phospho-p53 antibody (Ser15), rabbit anti-caspase-3 antibody, rabbit anti-phospho-NF-kB-p65 (Ser536) antibody, rabbit anti-NF-kB-p65 antibody (all Cell Signaling Technology Inc., Beverly, MA, USA), mouse anti-b-actin antibody (Sigma) or mouse anti-GAPDH antibody (Millipore, Billerica, USA) over night, followed by a 2 h incubation with anti-rabbit or anti-mouse IgG HRP-conjugated antibodies (Dako A/S, Glostrup, Denmark). Specific bands were visualized using ECL chemiluminescence substrate (Super Signal Pico, Pierce, USA) and CL-XPosure film (Thermo Scientific, Waltham, MA, USA).To assess the acute effects of the adipocytokines, human islets were incubated after a 2 day- pre-incubation and recovery period for 1 h at 2.8 mM glucose, followed by a 1 h-incubation period at 2.8 mM glucose plus adipocytokines 23977191 and an additional 1 hincubation period at 16.7 mM glucose plus adipocytokines. A second parallel experiment was designed to directly compare the adipocytokine effects after glucose stimulation. Human islets were acutely incubated with 2.8 mM for 1 h, followed by incubation at 16.7 mM glucose for 1 h and incubation at 16.7 mM glucose plus adipocytokines for 1 h. A third parallel experiment was designed to investigate whether adipokines also influence secretory machinery in general. Human islets were acutely incubated with 2.8 mM for 1 h, followed by incubation at in the presence of IBMX (100 uM) and Forskolin (10 uM, Sigma) as described before [30]. Islets were extracted with 0.18 N HCl in 70 ethanol for determination of insulin content. Islet i.Er panel) or a cytokine combination (10 ng/ml IL-1b+10 ng/ml IFN-c, middle and lower panel). Western blot analyses were performed for full length and cleaved caspase-3 (upper panel), phospho-NF-kB p65 (Ser536) and NF-kB p65 (middle panel) and phospho-p53 (Ser15) (lower panel). GAPDH or beta-actin were used as loading control. All panels show one typical blot out of three independent experiments. *p,0.05 compared to untreated control. doi:10.1371/journal.pone.0054106.gMeasurement of Intracellular NAD LevelThe concentrations of NAD in the whole cell extracts were analysed by a commercially available NAD/NADH assay kit ?(EnzyChromTM NAD/NADH Assay Kit; Koln, Germany). Therefore, 500,000 cells/well were seeded in 6well plates and cultured as described above. After treatment for 2 or 48 h, cells were trypsinized and 2 wells per sample were pooled and lysed in 100 ml NAD extraction buffer. To homogenize the samples, cell extracts were undergo freeze/thaw cycles. NAD level were determined according to manufacturer’s instructions. The cell pellet of each sample was resuspended in 100 ml 2 SDS, shaked for 10 min at 99uC and centrifuged for 5 min at 20,0006g and then used for protein determination (BCA Assay, Pierce Thermo Scientific). The NAD level of each sample was referred to the corresponding total protein amount of the sample.Western BlottingINS-1E cells were seeded into 6well plates at 500,000 cells/w ell and grown in culture medium. After 72 h, cells were incubated in serum free medium for 24 h. Thereafter, cells were incubated for 48 h for activated caspase-3, 6 h for p53 and 3 h for NF-kB detection under serum free conditions in the absence or presence of the treatment conditions. Equal amounts of protein from each treatment group were run on 10 or 15 SDS olyacrylamide gels. After semi-dry transfer onto nitrocellulose, membranes (0.45 mm) were blocked and subsequently incubated with rabbit anti-phospho-p53 antibody (Ser15), rabbit anti-caspase-3 antibody, rabbit anti-phospho-NF-kB-p65 (Ser536) antibody, rabbit anti-NF-kB-p65 antibody (all Cell Signaling Technology Inc., Beverly, MA, USA), mouse anti-b-actin antibody (Sigma) or mouse anti-GAPDH antibody (Millipore, Billerica, USA) over night, followed by a 2 h incubation with anti-rabbit or anti-mouse IgG HRP-conjugated antibodies (Dako A/S, Glostrup, Denmark). Specific bands were visualized using ECL chemiluminescence substrate (Super Signal Pico, Pierce, USA) and CL-XPosure film (Thermo Scientific, Waltham, MA, USA).To assess the acute effects of the adipocytokines, human islets were incubated after a 2 day- pre-incubation and recovery period for 1 h at 2.8 mM glucose, followed by a 1 h-incubation period at 2.8 mM glucose plus adipocytokines 23977191 and an additional 1 hincubation period at 16.7 mM glucose plus adipocytokines. A second parallel experiment was designed to directly compare the adipocytokine effects after glucose stimulation. Human islets were acutely incubated with 2.8 mM for 1 h, followed by incubation at 16.7 mM glucose for 1 h and incubation at 16.7 mM glucose plus adipocytokines for 1 h. A third parallel experiment was designed to investigate whether adipokines also influence secretory machinery in general. Human islets were acutely incubated with 2.8 mM for 1 h, followed by incubation at in the presence of IBMX (100 uM) and Forskolin (10 uM, Sigma) as described before [30]. Islets were extracted with 0.18 N HCl in 70 ethanol for determination of insulin content. Islet i.