Comparing with the expansion stage, %CD41 increased during differentiation stage from 13% to 19% for G1, while for G2 raised from 13% to 35%, but only from 17% to 19% for G3 (Fig. 3C). Over differentiation stage, the total number of cells increased about 3.7 folds for G1 (corresponding to 6.3 ± 1.0 × 106 total cells), and 4.4 folds for G2 (corresponding to 19 ± 4.2 × 106 total

cells), selleck screening library but only about 1.3 for G3 (corresponding to 26 ± 13 × 106 total cells). Scanning electron microscopy analysis showed similar morphology of culture-derived platelet-like particles and human PB-derived platelets (Fig. 4A, right and left, respectively), demonstrating the ability of the current protocol to support the in vitro production of platelet-like particles. Likewise, transmission electron microscopy (TEM) analysis of culture-derived Mk (Fig. 4B) showed normal features of a mature Mks with demarcation membrane (dm) system, nucleus (N) and α-granules characteristic

of such mature Mk. Electron microscopy (SEM and TEM) imaging was performed on 3 different populations from G2 and for each culture, platelet-like particles (similar to the Fig. 4A) was identified in more than 10 microscopy images. PD-1 inhibitor Ploidy analysis (Fig. 5A) revealed that about 18% of culture-derived Mks have higher ploidy (>4 N). Moreover, forward (FCS) and side scatter (SCC) properties of such population are higher compared to the CD41+ cells with 2 N and 4 N DNA content (Fig. 5B). Mks generated from UCB, compared to human PB, were described to be smaller and have less ploidy; however, as reported Phenylethanolamine N-methyltransferase previously [13] and confirmed in the current study, these are still able to produce platelets-like particles. The current study presents a two-stage protocol aiming at effective megakaryocytic differentiation of UCB CD34+-enriched cells. The results identified distinct individual groups which elucidate the relation between FI-CD34+ and efficiency of Mk production. This information is valuable to

balance the proliferation and differentiation potential of CD34+ cells, when targeting efficient Mk production. The underlying phenomena for such balance should be actually based in cell population doublings, but FI-CD34+ is a tangible parameter easier to quantify. Several studies have reported production of Mk cells and platelets from HSC/HCP. For example, using UCB progenitors, a perfusion system was used to produce enough number of platelets in vitro for clinical transfusion (300–600 × 109) [16]. However, the drawback of aforementioned work was most of culture-derived platelets were activated in the absence of any agonists. Another study reported producing 44 ± 8.1 Mks/input HSC/HPC using human mPB cells through a complex 3-step culture; includes a cocktail comprised by 17 different cytokines and changes in pH and O2 tension during experiment [17].