). Mature osteoclasts were seeded in 96-well plates as per the T cell activation assay. Autologous γδ and CD4+ T cells were labelled with 1 μM CellTrace™ CFSE (Molecular Probes) according to the manufacturer’s instructions, and 5 × 104 T cells (plus 100 U/ml IL-2) selleck products were cultured alone, or in the presence of osteoclasts,

for 5 days. Cultures were supplemented with fresh M-CSF and RANKL every 48 h to maintain osteoclast viability. In selected experiments, γδ T cells and CD4+ T cells were cultured with osteoclast conditioned medium for 5 days. γδ T cells and CD4+ T cells were then harvested and proliferation was assessed by quantifying CFSE fluorescence using an LSRII flow cytometer. Data were analysed with FlowJo software. To assess T cell survival in the absence or presence of osteoclasts, autologous γδ T cells and CD4+ T cells were co-cultured with osteoclasts for 5 days, at a T cell:osteoclast ratio of 5:1. In some experiments a monoclonal mouse anti-human TNFα neutralising antibody (or respective mouse IgG1, κ isotype control — both 10 μg/ml) was used to determine the

contribution of TNFα to the survival effects of osteoclasts on γδ T cells. Antibodies were pre-incubated with osteoclasts for 30 min prior to addition of γδ T cells. γδ T cells and CD4+ T cells were then harvested and stained with Annexin V-Pacific learn more Blue and 7-AAD (both eBioscience). T cell apoptosis/necrosis was assessed using flow cytometric analysis performed on an LSRII flow cytometer. Data were analysed with FlowJo software. Following co-culture of γδ and CD4+ T cells with autologous macrophages or osteoclasts for 3 days, T cells were harvested and stimulated with 50 ng/ml phorbol 12-myristate 13-acetate (PMA) and 1 μg/ml ionomycin ifenprodil in the presence of Golgistop reagent (BD Biosciences) for a further 6 h. γδ T cells and CD4+ T cells were then harvested and stained with anti-human γδ-TCR-FITC or anti-human CD4-FITC,

respectively, prior to fixation and permeabilisation with a Cytofix/Cytoperm kit (BD Biosciences). T cells were then stained using a monoclonal mouse anti-human IFNγ-V450 antibody or mouse IgG1, κ-V450 isotype control (both BD Biosciences), and monoclonal mouse anti-human-IL-17-PE or mouse IgG1-PE isotype control (both eBiosciences). IFNγ- and IL-17-producing T cells were then assessed using flow cytometric analysis with an LSR II flow cytometer, and data were analysed with FlowJo software. Data were analysed using the Kruskal–Wallis one-way analysis of variance on ranks (SigmaPlot®11.0), with inter-group comparisons analysed using the Wilcoxon matched-pairs rank test. p values ≤ 0.05 were considered statistically significant.