Figure 5
Figure 5. CD13+CD56−cells can give rise to NK cells. (A) Cells with distinct levels of CD13 expression: CD13low/neg (bottom), CD13intermediate (middle), and CD13high (top) were FACS purified from NK differentiation cultures (at day 14) and cultured further with cytokines and stroma. All 3 subsets gave rise to CD56+ NK cells, some of which coexpressed CD13. (B) Quantitative yield of CD56+ NK cells/104 CD13+ cells undergoing FACS. There was decreasing ability for NK-cell generation with increasing CD13 expression. A representative donor is shown (n = 4). Groups showing significant differences are indicated by asterisks (***P < .001, **P = .001-.01, and *P = .01-.05), 1-way analysis of variance on log-transformed values with Bonferroni posttest. (C) Freshly isolated GMPs (CD34+CD38+CD123+CD45RA−) were double-sorted from UCB and deposited into 96-well plates with stroma, HDC, and cytokines (FLT-3L, SCF, IL-7, and IL-15). After ∼ 21 days progeny were analyzed by FACS. Shown are the cells falling within the lymphoid gate by FSC versus SSC.

CD13+CD56cells can give rise to NK cells. (A) Cells with distinct levels of CD13 expression: CD13low/neg (bottom), CD13intermediate (middle), and CD13high (top) were FACS purified from NK differentiation cultures (at day 14) and cultured further with cytokines and stroma. All 3 subsets gave rise to CD56+ NK cells, some of which coexpressed CD13. (B) Quantitative yield of CD56+ NK cells/104 CD13+ cells undergoing FACS. There was decreasing ability for NK-cell generation with increasing CD13 expression. A representative donor is shown (n = 4). Groups showing significant differences are indicated by asterisks (***P < .001, **P = .001-.01, and *P = .01-.05), 1-way analysis of variance on log-transformed values with Bonferroni posttest. (C) Freshly isolated GMPs (CD34+CD38+CD123+CD45RA) were double-sorted from UCB and deposited into 96-well plates with stroma, HDC, and cytokines (FLT-3L, SCF, IL-7, and IL-15). After ∼ 21 days progeny were analyzed by FACS. Shown are the cells falling within the lymphoid gate by FSC versus SSC.

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