Necrosis was induced by pelleting cells followed by three cycles of freeze and thaw. Similar protocol was used for the induction of splenocyte apoptosis, which was isolated from spleens of C57BL/6 mice as described previously 34. Bone-marrow-derived immature live DC (100 000 cells/well) were co-cultured with apoptotic/necrotic DC or apoptotic splenocytes (1 000 000 cells/well). In some experiments, cytochalasin D (0.8 μg/mL) was added to

inhibit phagocytosis. In order to inhibit mTOR signaling pathway, rapamycin (100 nm) was added to the co-culture of apoptotic DC with viable DC. Twenty-four hours later, cells were exposed to 1 μg/mL LPS, and FACS analysis was performed. Live DC (100 000/well) were incubated with apoptotic/necrotic DC or apoptotic splenocytes (1 000 000 cells/well) at a ratio of 1:10 and then pulsed with OVA, followed by co-culture with naïve CD4+ T cells (250 000/well) selleck screening library from OT-II mice. Five days Ivacaftor purchase later, CD4+ T cells were analyzed for foxp3 expression via FACS. In some experiments, neutralizing TGF-β Ab was added (50 μg/mL). In transwell experiments, DC were added to the top chamber and naïve CD4+ T cells from C57BL/6 mice were placed in the lower chamber and stimulated with plate bound CD3 and

soluble CD28 antibodies OVA-pulsed (0.5 mg/mL) DC were used as stimulators and naïve OT-II CD4+ T cells were used as responders. The stimulators (2.5×105 cells/well) and responder cells (2.5×104 cells/well) were cultured in 96-well round-bottom plates at a ratio of 10:1 and suppressors (CD25+) isolated from co-culture of OT-II naïve T cells, and OVA-pulsed viable DC that had taken up apoptotic DC were added. Proliferation was RAS p21 protein activator 1 assessed at day 4 of co-culture using BrdU cell proliferation assay following the manufacturer’s instructions (Roche, QC). Naïve CD4+CD25– T cells were cultured for 4 days in the presence of LPS-treated live DC, LPS-treated live DC incubated with necrotic DC or LPS-treated live DC incubated with apoptotic

DC, and were activated with plate-bound anti-CD3 and soluble anti-CD28 antibodies in the presence of 5 ng/mL IL-6, 2.5 ng/mL TGF-β, 10 μg/mL anti-IL-4 and 10 μg/mL anti-IFN-γ. We quantified the levels of total/active TGF-β1 in culture supernatants by ELISA using commercial kit following the manufacturer’s instructions (TGF-β1 kit, R&D Systems). However, for the measurements of TGF-β, cells were cultured in X-VIVO 20 serum-free medium (Cambrex). TaqMan real-time RT-PCR was carried out as described previously using primer sequences listed in Table 1 36. Statistical analyses were performed using Student’s t-test to compare two groups and ANOVA to compare multiple groups (SPSS 16.0). Significance was set at p<0.05. This work was supported in part by Operating Grants from the Canadian Institutes of Health Research, the Canadian Cystic Fibrosis Foundation, and the Foundation Fighting Blindness-Canada to J. H. J. H.