Ells. Moreover we analysed the biological characteristics of the artificial construct and this enabled us to order AKT inhibitor 2 hypothesize why providing a three-dimensional cellular architecture is essential to recreate the unique functions and characteristics of the thymic environment in vitro.Materials and MethodsEthics statementCord blood samples were collected from consenting mothers following birth and adult blood by venepuncture from a 55 years old adult donor following 3PO chemical information ethical permission by The Royal Marsden Local research Ethics Committee. The participants provided written informed 10457188 consent.CD34+ cell separationMononuclear cells were separated from whole blood by gradient centrifugation using Ficoll-Paque (GE Heatlhcare) and subsequently depleted of CD2 and CD20 cells and enriched for CD34 using Microbeads (Miltenyi) 16574785 according to MACS methodHuman T Lineage Development In VitroFigure 2. Kinetics of thymocytes generation. . (A) By day 5 CD4 dimintermediate single positive and some double positive CD4+CD8+ cells were present. These progenitors all expressed CD45, either high or dim and analysis of cultures also showed the presence of CD1a+CD7+ and CD1a+CD7 cells The images are representative of three different experiments.doi: 10.1371/journal.pone.0069572.gon a VarioMACS magnet [10]. The separated cells were analyzed by flow cytometry and consisted of a unique highly pure CD34+CD45lo population. Purity (considered as CD34 expression out of total CD45) was always > 90 in all separations, and viability, evaluated by staining the cells with 250 ng/ml Propidium Iodide solution (Sigma Aldricht), always >99 , No CD3 nor CD20 contaminating lymphocytes were detected. These freshly separated and collected CD34+cells were then used for the T cell differentiation studies.Culture of keratinocytes and fibroblastsThe HaCaT cell line (CLS, DKFZ) [11] were cultured in DMEM medium (Sigma-Aldrich) supplemented with 10 heatinactivated fetal bovine serum (FBS), 2mM L-glutamine and 10 antibiotics (penicillin 100U/ml and streptomycin 100mg/ml) at 37 with 5 CO2. The cells were passaged when less than 80 confluence. Primary Fibroblasts were purchased from Invitrogen, and cultured in Medium 106 (Invitrogen) supplemented with 2 heat-inactivated fetal bovine serum (FBS), hydrocortisone 1mg/ml, human-Epithelial Growth Factor 10ng/ml, human-basic Fibroblasts Growth Factor 3ng/ml, heparin 10 /ml and 1X gentamycin/amphotericin. Thefibroblasts were used at less than 15 passages. Threedimensional skin constructs were performed on 9-mm ?9-mm ?1.5-mm tantalum coated carbon Cellfoam matrices (Cytomatrix) incubated with 100 /ml rat tail collagen I (Sigma Aldricht) and seeded with 1×105 HaCaT Keratinocytes and 5?04 primary fibroblasts, in culture medium consisting of a 1:1 mixture of the fibroblast and keratinocyte media described above. After 5 hours at 37 , 5 CO2, matrices were moved to a new 24-well plate and 2 ml of a 1:1 mixture of the two media described above was added. The skin cell constructs were cultured for 6 days and medium was changed every other day. On day 6, CD34 cells, isolated from either umbilical cord or adult peripheral blood, were added to each matrix, and the unit cultured in DMEM supplemented with 10 heat-inactivated FCS (Sigma-Aldrich), 20 ng/ml IL-7 (Miltenyi), 20 ng/ml IL-15 (Miltenyi), 100 ng/ml Flt-3L ligand (Miltenyi) and penicillin/ streptomycin (Sigma-Aldrich). One-half of the medium was aspirated and replaced every 3 days, and the coculture mai.Ells. Moreover we analysed the biological characteristics of the artificial construct and this enabled us to hypothesize why providing a three-dimensional cellular architecture is essential to recreate the unique functions and characteristics of the thymic environment in vitro.Materials and MethodsEthics statementCord blood samples were collected from consenting mothers following birth and adult blood by venepuncture from a 55 years old adult donor following ethical permission by The Royal Marsden Local research Ethics Committee. The participants provided written informed 10457188 consent.CD34+ cell separationMononuclear cells were separated from whole blood by gradient centrifugation using Ficoll-Paque (GE Heatlhcare) and subsequently depleted of CD2 and CD20 cells and enriched for CD34 using Microbeads (Miltenyi) 16574785 according to MACS methodHuman T Lineage Development In VitroFigure 2. Kinetics of thymocytes generation. . (A) By day 5 CD4 dimintermediate single positive and some double positive CD4+CD8+ cells were present. These progenitors all expressed CD45, either high or dim and analysis of cultures also showed the presence of CD1a+CD7+ and CD1a+CD7 cells The images are representative of three different experiments.doi: 10.1371/journal.pone.0069572.gon a VarioMACS magnet [10]. The separated cells were analyzed by flow cytometry and consisted of a unique highly pure CD34+CD45lo population. Purity (considered as CD34 expression out of total CD45) was always > 90 in all separations, and viability, evaluated by staining the cells with 250 ng/ml Propidium Iodide solution (Sigma Aldricht), always >99 , No CD3 nor CD20 contaminating lymphocytes were detected. These freshly separated and collected CD34+cells were then used for the T cell differentiation studies.Culture of keratinocytes and fibroblastsThe HaCaT cell line (CLS, DKFZ) [11] were cultured in DMEM medium (Sigma-Aldrich) supplemented with 10 heatinactivated fetal bovine serum (FBS), 2mM L-glutamine and 10 antibiotics (penicillin 100U/ml and streptomycin 100mg/ml) at 37 with 5 CO2. The cells were passaged when less than 80 confluence. Primary Fibroblasts were purchased from Invitrogen, and cultured in Medium 106 (Invitrogen) supplemented with 2 heat-inactivated fetal bovine serum (FBS), hydrocortisone 1mg/ml, human-Epithelial Growth Factor 10ng/ml, human-basic Fibroblasts Growth Factor 3ng/ml, heparin 10 /ml and 1X gentamycin/amphotericin. Thefibroblasts were used at less than 15 passages. Threedimensional skin constructs were performed on 9-mm ?9-mm ?1.5-mm tantalum coated carbon Cellfoam matrices (Cytomatrix) incubated with 100 /ml rat tail collagen I (Sigma Aldricht) and seeded with 1×105 HaCaT Keratinocytes and 5?04 primary fibroblasts, in culture medium consisting of a 1:1 mixture of the fibroblast and keratinocyte media described above. After 5 hours at 37 , 5 CO2, matrices were moved to a new 24-well plate and 2 ml of a 1:1 mixture of the two media described above was added. The skin cell constructs were cultured for 6 days and medium was changed every other day. On day 6, CD34 cells, isolated from either umbilical cord or adult peripheral blood, were added to each matrix, and the unit cultured in DMEM supplemented with 10 heat-inactivated FCS (Sigma-Aldrich), 20 ng/ml IL-7 (Miltenyi), 20 ng/ml IL-15 (Miltenyi), 100 ng/ml Flt-3L ligand (Miltenyi) and penicillin/ streptomycin (Sigma-Aldrich). One-half of the medium was aspirated and replaced every 3 days, and the coculture mai.
