Ons; PBMC alone, 0.3 mg/ml aCD3 (eBioscience; Clone HIT3a) or 0.3 mg/ml aCD3+1 mg/ml aCD28 (eBioscience; Clone CD28.2). The co-cultures were incubated for 6 days at 37uC. After 6 days in culture the nonadherent cells were then collected for staining and flow cytometric analysis. Non-adherent cells were stained with PE conjugated Docosahexaenoyl ethanolamide web antihuman CD4 (eBioscience; Clone OKT4) and PE-Cy5 anti-human CD8a (Biolegend; Clone HIT8a) prior to multi-colour flow cytometric analysis. T cell proliferation was then quantitated with the parameters set to a log scale. A forward scatter 
vs FL1 was used to gate on the PBMC population that was positive for CFSE. This gated population was then used to differentiate between CD4+ T cells and CD8+ T cells. CFSE histograms depict the number of events (y-axis) and the fluorescence intensity (x-axis) with proliferating cells displaying a progressive 2-fold loss in fluorescence intensity following cell division, indicative of proliferating cells. To determine whether cell contact is necessary for EC to support T cell proliferation, the use of transwells was employed. 16105 PBMC/well were placed in 0.4 mm transwells (Costar) and co-culture with HBEC performed as outlined above.Cells and cell cultureImmortalised human brain microvascular hCMEC/D3 endothelial cells (HBEC) [18] were cultured in EBM-2 medium (Lonza CC-3156). Cells were grown on plates pre-coated with rat tail collagen type I (BD Biosciences). Cytokine activation of HBEC was performed by treating the 
cells with 10 ng/ml TNF or 50 ng/ ml IFNc (Peprotech) for 18 h.Human PBMC preparationPBMC were separated either from leukopacks or from heparinized venous blood by conventional Ficoll gradient and brought to 26106/ml in complete medium. PBMC were frozen in 10 DMSO in FCS and stored in liquid nitrogen. PBMC were thawed and washed twice in cold medium before use in assays.T cell isolation and CFSE stainingCD4+ and CD8+ T cells were isolated from freshly thawed PBMCs using an EasysepH (Stemcell Technologies) negative selection kit according to the manufacturer’s instructions. For labeling both isolated T cells and whole PBMCs with Carboxyfluorescein succinimidyl ester (CFSE; Invitrogen), cells (at a density of 107 cells/ml) were incubated for 10 min at 37uC in 5 mM CFSE in serum free RPMI. The labelling reaction was stopped by the addition of serum. Cells were then washed 3 times prior to use. For the quantification of cell proliferation, cells were analysed by flow cytometry with a reduction in CFSE MFI indicative of 1326631 cell division.MHC II expression on HBEC following co-cultureTo assess the expression of MHC II on HBEC following INCB039110 biological activity coculture with PBMC, HBEC were removed by trypsinisation following 6 d of co-culture. HBEC were then stained with antihuman MHC II (HLA-DR; eBioscience). For flow cytometric analysis CFSE positive cells (PBMC) were excluded by gating to ensure MHC II analysis was conducted on HBEC only.Flow cytometryFor multicolor flow cytometric analysis, HBEC were incubated in the presence of fluorochrome-conjugated mAbs against CD105 (SN6), CD106 (STA), CD80 (2D10.4), CD86 (IT2.2), CD40 (5C3), HLA-DR/MHC II (LN3) and CD275 (MIH12) (all from eBioscience), CD54 (5.6E; Beckman Coulter) and b2-microglobu?lin/MHC I (TU99; BD Biosciences) as per manufacturer’s instructions.Results HBEC express key molecules for antigen presentation and T cell activationFor this study we employed a particular line of immortalized human microvascular EC (HBEC; hCMEC/D3) that re.Ons; PBMC alone, 0.3 mg/ml aCD3 (eBioscience; Clone HIT3a) or 0.3 mg/ml aCD3+1 mg/ml aCD28 (eBioscience; Clone CD28.2). The co-cultures were incubated for 6 days at 37uC. After 6 days in culture the nonadherent cells were then collected for staining and flow cytometric analysis. Non-adherent cells were stained with PE conjugated antihuman CD4 (eBioscience; Clone OKT4) and PE-Cy5 anti-human CD8a (Biolegend; Clone HIT8a) prior to multi-colour flow cytometric analysis. T cell proliferation was then quantitated with the parameters set to a log scale. A forward scatter vs FL1 was used to gate on the PBMC population that was positive for CFSE. This gated population was then used to differentiate between CD4+ T cells and CD8+ T cells. CFSE histograms depict the number of events (y-axis) and the fluorescence intensity (x-axis) with proliferating cells displaying a progressive 2-fold loss in fluorescence intensity following cell division, indicative of proliferating cells. To determine whether cell contact is necessary for EC to support T cell proliferation, the use of transwells was employed. 16105 PBMC/well were placed in 0.4 mm transwells (Costar) and co-culture with HBEC performed as outlined above.Cells and cell cultureImmortalised human brain microvascular hCMEC/D3 endothelial cells (HBEC) [18] were cultured in EBM-2 medium (Lonza CC-3156). Cells were grown on plates pre-coated with rat tail collagen type I (BD Biosciences). Cytokine activation of HBEC was performed by treating the cells with 10 ng/ml TNF or 50 ng/ ml IFNc (Peprotech) for 18 h.Human PBMC preparationPBMC were separated either from leukopacks or from heparinized venous blood by conventional Ficoll gradient and brought to 26106/ml in complete medium. PBMC were frozen in 10 DMSO in FCS and stored in liquid nitrogen. PBMC were thawed and washed twice in cold medium before use in assays.T cell isolation and CFSE stainingCD4+ and CD8+ T cells were isolated from freshly thawed PBMCs using an EasysepH (Stemcell Technologies) negative selection kit according to the manufacturer’s instructions. For labeling both isolated T cells and whole PBMCs with Carboxyfluorescein succinimidyl ester (CFSE; Invitrogen), cells (at a density of 107 cells/ml) were incubated for 10 min at 37uC in 5 mM CFSE in serum free RPMI. The labelling reaction was stopped by the addition of serum. Cells were then washed 3 times prior to use. For the quantification of cell proliferation, cells were analysed by flow cytometry with a reduction in CFSE MFI indicative of 1326631 cell division.MHC II expression on HBEC following co-cultureTo assess the expression of MHC II on HBEC following coculture with PBMC, HBEC were removed by trypsinisation following 6 d of co-culture. HBEC were then stained with antihuman MHC II (HLA-DR; eBioscience). For flow cytometric analysis CFSE positive cells (PBMC) were excluded by gating to ensure MHC II analysis was conducted on HBEC only.Flow cytometryFor multicolor flow cytometric analysis, HBEC were incubated in the presence of fluorochrome-conjugated mAbs against CD105 (SN6), CD106 (STA), CD80 (2D10.4), CD86 (IT2.2), CD40 (5C3), HLA-DR/MHC II (LN3) and CD275 (MIH12) (all from eBioscience), CD54 (5.6E; Beckman Coulter) and b2-microglobu?lin/MHC I (TU99; BD Biosciences) as per manufacturer’s instructions.Results HBEC express key molecules for antigen presentation and T cell activationFor this study we employed a particular line of immortalized human microvascular EC (HBEC; hCMEC/D3) that re.
