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. 2010 Feb 15;5(2):e9221. doi: 10.1371/journal.pone.0009221

Table 2. Overview of CD34+ cell selections and NK cell culturing procedures.

Method I - H3000 Method I - Stemline I Method I - Stemline II
CD34 (%) CD34 cells (×106) CD56 (%) CD56 cells (×109) CD56 (%) CD56 cells (×109) CD56 (%) CD56 cells (×109)
UCB1 78 1.10 50 0.57 74 1.20 87 2.20
UCB2 55 0.32 88 0.68 65 0.15 82 0.15
UCB3 93 0.52 94 3.10 43 0.55 71 0.50
UCB4 69 0.45 n.d. n.d. 99 3.50 57 0.12
UCB5 87 0.20 n.d. n.d. 75 0.40 48 0.02
UCB6 83 0.94 n.d. n.d. 97 10.0 49 0.12
mean 78 0.59 77 1.50 75 2.70 66 0.51
SD 14 0.36 24 0.14 21 4.00 17 0.82
range 55–93 0.20–1.10 50–94 0.57–3.10 43–99 0.15–10.0 48–87 0.02–2.20
median 81 0.49 88 0.68 75 0.90 64 0.14

Table 2 shows a summary of all different experiments and the corresponding UCB donors using the different culture methods I–III and media (see Figure 1). The purity and the total number of CD34+ cells after immunomagnetic selection determined by FCM are depicted for each UCB donor. The CD56 content after 5 weeks (Method I and II) or 6 weeks (Method III) of culture was analyzed by FCM as described in Materials and Methods. Numbers of NK cells represent a theoretical calculation based on the actual expansion rates of CD56+ NK cells and were calculated using the initial numbers of CD34+ cells from each UCB multiplied by the NK cell expansion rate from each culture procedure. The mean ± standard deviation (SD), range and median are calculated for each method and medium separately.