R each experiment.Immunophenotypic analysis of TNCsWe characterised the antigenic phenotype

R each experiment.Immunophenotypic analysis of TNCsWe characterised the antigenic phenotype of the TNCs by flow cytometry focusing on the Lin2CD452 cell fraction. Standard flow cytometry-based protocols for HSC usually exclude events smaller than 6 mm as this fraction is mainly composed of erythrocytes, platelets, and cellular debris [19,20]. As previous reports suggested that Lin2CD452 cells are smaller than HSC, with a size between 2? mm [3,4,5], we applied a log scale to the Forward scatter to including events smaller than 6 mm using beads as size markers. When events starting from 3 mm were included (Figure 2A), cells positive for Lin and CD41a, a specific platelet marker, were excluded by gating (Figure 2B); expression of CD45, CD133, CD34, CXCR4 and Nestin was assessed in the Lin2 gateResults Recovery of the Lin2CD452 Fraction from Cord Blood Total Nucleated Cells (TNCs) using either Lysis or FicollWe assessed whether recovery of the Lin2CD452 fraction differed when lysing buffer or Ficoll density centrifugation were used to prepare TNCs. As shown in Fig. 1A, the percentage of Lin2CD452 cells recovered was significantly lower (p = 0.0025)hUCB ELSc Are a Heterogeneous PopulationFigure 4. Heterogeneity of the Lin2CD452 population. (A) SSC and FSC back gate show CXCR4+, CD34+, and Nestin+ subpopulations compared to specific size beads of 6 mm and the Lin2CD45dimCD34+ (black); they have the same range of size in FSC but are allocated differently in SSC. (B) The box plot shows the percentage of CD34+, CXCR4+ and Nestin+ cells; note that Nestin+ cells are the larger population within the Lin2CD452 cell fraction. (n = 4; *p,0.05/**p,0.005). (C) Gate shows that CXCR4+ cells are negative for 1315463 CD34 (D) Gate shows Nestin+ CD342 and Nestin+ CD34+ cells. (C and D percentages represent the mean from 4 different samples). doi:10.1371/journal.pone.0067968.gseparately in SIS-3 samples (Fig. 2C ). The Lin2CD452 population expressed CD34, CXCR4, and Nestin, but not CD133.Characterisation of the Lin2CD452 Cell FractionThe Lin2CD452 population was further characterized by flow cytometry, immunocytochemistry and RT-PCR. Flow cytometry showed that CD34, CXCR4, and Nestin positive cells were consistently detected in all cell preparations (n = 4; Fig. 3C ); in contrast, detection of CD133 was a rare event and most samples were negative (,0.03 , n = 4; Fig. 3F). Interestingly, Nestin+ and CD34+ cells were different in size from CXCR4 cells, as assessed by SSC and FSC (Fig. 4A). In doublestaining experiments it was found that cells positive for CXCR4 were negative for CD34 (Fig. 4C), while approximately 21 of Nestin positive cells were also positive for CD34 (20.9767.242 N = 4; Fig. 4D). Finally of note, a high proportion of events were either very small, on the edge of the 2 mm threshold (80 ), or not stained by any antibody used; these could represent cellular debris. The Lin2CD452 populations were separately Nafarelin back-gated for SSC and FSC to compare them with the Lin2CD45dimCD34+population using beads as size markers. The Lin2CD452 cells were found to be smaller than Lin2CD45dimCD34+ cells by SSC and FSC (Fig. 4A). Expression of the pluripotent markers, SSEA-4, Sox2, and Oct3/4, in the Lin2CD452 fraction was investigated by using flow cytomery. SSEA-4 was expressed in 260.3498 (N = 5) of the cells and Oct3/4 in less than 1 (Fig. 5B ). Sox2 was not found expressed by flow cytometry (Fig. 5A). Of note, the SSEA-4 positive cells were negative for CD34 and CD133. Th.R each experiment.Immunophenotypic analysis of TNCsWe characterised the antigenic phenotype of the TNCs by flow cytometry focusing on the Lin2CD452 cell fraction. Standard flow cytometry-based protocols for HSC usually exclude events smaller than 6 mm as this fraction is mainly composed of erythrocytes, platelets, and cellular debris [19,20]. As previous reports suggested that Lin2CD452 cells are smaller than HSC, with a size between 2? mm [3,4,5], we applied a log scale to the Forward scatter to including events smaller than 6 mm using beads as size markers. When events starting from 3 mm were included (Figure 2A), cells positive for Lin and CD41a, a specific platelet marker, were excluded by gating (Figure 2B); expression of CD45, CD133, CD34, CXCR4 and Nestin was assessed in the Lin2 gateResults Recovery of the Lin2CD452 Fraction from Cord Blood Total Nucleated Cells (TNCs) using either Lysis or FicollWe assessed whether recovery of the Lin2CD452 fraction differed when lysing buffer or Ficoll density centrifugation were used to prepare TNCs. As shown in Fig. 1A, the percentage of Lin2CD452 cells recovered was significantly lower (p = 0.0025)hUCB ELSc Are a Heterogeneous PopulationFigure 4. Heterogeneity of the Lin2CD452 population. (A) SSC and FSC back gate show CXCR4+, CD34+, and Nestin+ subpopulations compared to specific size beads of 6 mm and the Lin2CD45dimCD34+ (black); they have the same range of size in FSC but are allocated differently in SSC. (B) The box plot shows the percentage of CD34+, CXCR4+ and Nestin+ cells; note that Nestin+ cells are the larger population within the Lin2CD452 cell fraction. (n = 4; *p,0.05/**p,0.005). (C) Gate shows that CXCR4+ cells are negative for 1315463 CD34 (D) Gate shows Nestin+ CD342 and Nestin+ CD34+ cells. (C and D percentages represent the mean from 4 different samples). doi:10.1371/journal.pone.0067968.gseparately in samples (Fig. 2C ). The Lin2CD452 population expressed CD34, CXCR4, and Nestin, but not CD133.Characterisation of the Lin2CD452 Cell FractionThe Lin2CD452 population was further characterized by flow cytometry, immunocytochemistry and RT-PCR. Flow cytometry showed that CD34, CXCR4, and Nestin positive cells were consistently detected in all cell preparations (n = 4; Fig. 3C ); in contrast, detection of CD133 was a rare event and most samples were negative (,0.03 , n = 4; Fig. 3F). Interestingly, Nestin+ and CD34+ cells were different in size from CXCR4 cells, as assessed by SSC and FSC (Fig. 4A). In doublestaining experiments it was found that cells positive for CXCR4 were negative for CD34 (Fig. 4C), while approximately 21 of Nestin positive cells were also positive for CD34 (20.9767.242 N = 4; Fig. 4D). Finally of note, a high proportion of events were either very small, on the edge of the 2 mm threshold (80 ), or not stained by any antibody used; these could represent cellular debris. The Lin2CD452 populations were separately back-gated for SSC and FSC to compare them with the Lin2CD45dimCD34+population using beads as size markers. The Lin2CD452 cells were found to be smaller than Lin2CD45dimCD34+ cells by SSC and FSC (Fig. 4A). Expression of the pluripotent markers, SSEA-4, Sox2, and Oct3/4, in the Lin2CD452 fraction was investigated by using flow cytomery. SSEA-4 was expressed in 260.3498 (N = 5) of the cells and Oct3/4 in less than 1 (Fig. 5B ). Sox2 was not found expressed by flow cytometry (Fig. 5A). Of note, the SSEA-4 positive cells were negative for CD34 and CD133. Th.