Option (Becton Dickinson, San Diego, CA), in order to enumerate the

Option (Becton Dickinson, San Diego, CA), in order to enumerate the circulating EPC (CD34+/CD133+/VEGFR-2+/CD45- cells). Appropriate gate analysis was used for the detection of EPC excluding events of different origin, such as non-hematopoietic circulating cells and non-specifically stained events. At least 200.000 events were analyzed for each sample. The following antibodies (Ab) were used for FACS analysis: Flk-1/VEGF-R2 rabbit polyclonal IgG (Santa Cruz Biotechnology; Santa Cruz, CA) followed by anti-rabbit FITC Ab (DAKO, Milan, Italy); CD133 Ab (AC-133 PE; Miltenyi Biotech, Auburn, CA), CD45 Ab (2D1 APC or 2D1PercP; BD Biosciences Pharmingen,) and CD34 Ab (Q-Bend/10 PercP or QBend/10 APC; BD Biosciences Pharmingen).Fluorescence in situ hybridization (FISH)FISH analysis was carried out using an enumeration probe (i.e. Centromeric Probe CEP6 and CEP9) for a ploidy chromosome 23727046 set evaluation. The probes were chosen from a commercially available list “Vysis FISH Chromosome probes” provided by Abbott Molecular (Abbott Park, IL). The FISH procedure was performed according to the manufacturer’s protocol. For each probe, 100 cells were evaluated. The cells were viewed through an epifluorescent microscope equipped with 100X oil objective lens and triple bandpass filter for DAPI, SpectrumGreen and SpectrumOrange.Immunocytochemical analysisImmunohistochemistry analysis was carried out by performing the alkaline phosphatase anti-alkaline-phosphatase (APAAP) staining, as previously described [26,27], using the following monoclonal Ab: Factor VIII Ab (F8/86; DAKO), CD31 (WM-59; BD), VEGF receptor-2 (KDR-1; MedChemExpress GSK429286A Sigma-Chemical, St. Louis, MO), CD105 (8E11; Cymbus Biotechnology); CD106 (1G1b1; Valter Occhiena, Torino, Italy), CD14 (MWP9; BD), and CD45 (HI30; BD). EPC/ECFC were identified on the basis of their positivity for: Factor VIII, CD31, VEGFR-2, CD105, CD106, and negativity for CD14 and CD45 markers.Cytokines assayPeripheral blood mononuclear cell (PBMC) suspensions were isolated by density-gradient centrifugation with lymphocyte cell separation medium (Cedarlane Laboratories, Hornby, Ontario, Canada). Patient PBMC were then seeded at a cell density of 2.56106/ml in serum free Iscove medium (Gibco BRL, Grand Island, NY) supplemented with 1 penicillin/streptomycin and 2 L-glutamine. After 48 hours of culture at 37uC in 5 CO2, PBMC conditioned supernatants were collected by centrifugation, followed by filtration through 0,22mm Millipore sterile filters (Millipore Corporation, Bedford, MA, USA), and froze at -20 uC. Samples were assessed in duplicate for the determination of angiogenic cytokine GSK3326595 biological activity levels by using a searchlight human angiogenesis array 3-multiplex assay (Aushon Biosystems, Billerica, MA). Sensitivity of the assay was: 3.7 pg/ml for HB-EGF, 1.95 pg/ml for KGF and PDGF-AA, 11.7 pg/ml for TPO, 21.5 pg/ml for VEGFR-1 and 27.3 pg/ml for VEGFR-2.Single cell clonogenic assayWhen primary colonies reached a size with more than 100 cells/colony, adherent cells were detached by using trypsin/EDTA (Gibco BRL), re-suspended in complete EGM-2 medium, and subcultured by seeding no more then 1 cell/well in a collagen I 96well tissue culture dishes. Medium was changed every 3 days. Individual wells were daily examined under the microscope to score the number of cells growing per well. Subclones were classified on the basis of their in vitro expansion and progeny capacity, in agreement with the study of Barrandon and GreenEndothelial Progenitor Cell.Option (Becton Dickinson, San Diego, CA), in order to enumerate the circulating EPC (CD34+/CD133+/VEGFR-2+/CD45- cells). Appropriate gate analysis was used for the detection of EPC excluding events of different origin, such as non-hematopoietic circulating cells and non-specifically stained events. At least 200.000 events were analyzed for each sample. The following antibodies (Ab) were used for FACS analysis: Flk-1/VEGF-R2 rabbit polyclonal IgG (Santa Cruz Biotechnology; Santa Cruz, CA) followed by anti-rabbit FITC Ab (DAKO, Milan, Italy); CD133 Ab (AC-133 PE; Miltenyi Biotech, Auburn, CA), CD45 Ab (2D1 APC or 2D1PercP; BD Biosciences Pharmingen,) and CD34 Ab (Q-Bend/10 PercP or QBend/10 APC; BD Biosciences Pharmingen).Fluorescence in situ hybridization (FISH)FISH analysis was carried out using an enumeration probe (i.e. Centromeric Probe CEP6 and CEP9) for a ploidy chromosome 23727046 set evaluation. The probes were chosen from a commercially available list “Vysis FISH Chromosome probes” provided by Abbott Molecular (Abbott Park, IL). The FISH procedure was performed according to the manufacturer’s protocol. For each probe, 100 cells were evaluated. The cells were viewed through an epifluorescent microscope equipped with 100X oil objective lens and triple bandpass filter for DAPI, SpectrumGreen and SpectrumOrange.Immunocytochemical analysisImmunohistochemistry analysis was carried out by performing the alkaline phosphatase anti-alkaline-phosphatase (APAAP) staining, as previously described [26,27], using the following monoclonal Ab: Factor VIII Ab (F8/86; DAKO), CD31 (WM-59; BD), VEGF receptor-2 (KDR-1; Sigma-Chemical, St. Louis, MO), CD105 (8E11; Cymbus Biotechnology); CD106 (1G1b1; Valter Occhiena, Torino, Italy), CD14 (MWP9; BD), and CD45 (HI30; BD). EPC/ECFC were identified on the basis of their positivity for: Factor VIII, CD31, VEGFR-2, CD105, CD106, and negativity for CD14 and CD45 markers.Cytokines assayPeripheral blood mononuclear cell (PBMC) suspensions were isolated by density-gradient centrifugation with lymphocyte cell separation medium (Cedarlane Laboratories, Hornby, Ontario, Canada). Patient PBMC were then seeded at a cell density of 2.56106/ml in serum free Iscove medium (Gibco BRL, Grand Island, NY) supplemented with 1 penicillin/streptomycin and 2 L-glutamine. After 48 hours of culture at 37uC in 5 CO2, PBMC conditioned supernatants were collected by centrifugation, followed by filtration through 0,22mm Millipore sterile filters (Millipore Corporation, Bedford, MA, USA), and froze at -20 uC. Samples were assessed in duplicate for the determination of angiogenic cytokine levels by using a searchlight human angiogenesis array 3-multiplex assay (Aushon Biosystems, Billerica, MA). Sensitivity of the assay was: 3.7 pg/ml for HB-EGF, 1.95 pg/ml for KGF and PDGF-AA, 11.7 pg/ml for TPO, 21.5 pg/ml for VEGFR-1 and 27.3 pg/ml for VEGFR-2.Single cell clonogenic assayWhen primary colonies reached a size with more than 100 cells/colony, adherent cells were detached by using trypsin/EDTA (Gibco BRL), re-suspended in complete EGM-2 medium, and subcultured by seeding no more then 1 cell/well in a collagen I 96well tissue culture dishes. Medium was changed every 3 days. Individual wells were daily examined under the microscope to score the number of cells growing per well. Subclones were classified on the basis of their in vitro expansion and progeny capacity, in agreement with the study of Barrandon and GreenEndothelial Progenitor Cell.