This observation is highlighted when two populations of CD34+-enriched cells from the same UCB were cultured; one of this populations was expanded with a FI-CD34+ in the

range of G2 (FI-CD34+:15.1) and another one in the range of G3 (FI-CD34+:60). The first experiment resulted in EY of 67 with 25% CD41+ cells though the second experiment resulted in a lower EY and %CD41 (38 and 5.9%, respectively). Considering that the FI-CD34+ is related with cell population doublings, in an idealized cell population, a FI-CD34+ of 16 and 64 would correspond to 4 and 6 cell population doublings, respectively. Different factors can contribute to the loss of Mk differentiation potential for G3, namely cell commitment toward the granulocytic and monocytic lineage (24.0 ± 4.3% CD14+ cells) [12], NVP-BGJ398 ic50 or neutrophil lineages (64.0 ± 12.1% HLA-DR++ CD117++) [14]. As a control, UCB CD34+-enriched Wnt inhibitor cells were expanded in the same culture conditions, but in absence of feeder layer; regardless the different conditions

tested, both FI-CD34+ and EY were maintained at low levels (2.7 ± 0.91 and 7.0 ± 1.2, respectively; n = 3). It has been previously reported that FI-CD34+ was consistently lower in the absence of feeder [12] and [15]. Therefore, this result highlighted the positive effect of presence of feeder layer, in the expansion stage, when targeting an efficient Mk differentiation. Boyer and colleagues have previously suggested a 5-day expansion period as optimal for the increased production of Mks from UCB CD34+ cells (>95% enriched) in a two-phase protocol. However, using FI-CD34+ in the expansion stage as an operational parameter, rather than the expansion

duration, has more advantages such as considering the intrinsic biological variability of UCB samples and the impact of initial CD34+ enrichment. The current study thus demonstrated that by using FI-CD34+, as a key parameter, we were able to determine the effectiveness Branched chain aminotransferase of megakaryocyte differentiation of UCB cells, identifying different groups with statistical significance (G1, G2 and G3 in Fig. 2A and C in terms of FI-CD34+, p < 0.05). Indeed, such identification would not be statistically significant if expansion duration was used instead ( Fig. 2B and D; p > 0.3 between G1, G2 and G3 in terms of expansion duration). In the current study, the initial population consisted of 1.5 × 105 cells with similar cell population compositions (Fig. 3). At the end of the expansion, the total numbers of cells were 1.7 ± 0.40 × 106, 4.2 ± 0.30 × 106 and 20 ± 9.1 × 106 for G1, G2 and G3, respectively. In the expansion stage, the reduction in %CD34 (from 90 to 65% for G1, from 83% to 51% for G2 and from 77% to 36% for G3) was accompanied by an increase in %CD33 (early myeloid cells), from 56% to 83% for G1, from 52% to 91% for G2 and from 53% to 92% for G3. A significant decrease in %CD34 was observed during the differentiation stage (from 65% to 2.9% for G1, 51–2.5% for G2 and 36–5% for G3, Fig. 3A and B).