Figure 4.
Figure 4. In vitro differentiation of human NK cells derived from FACS sorter-purified progenitor cells of NOD/SCID mouse BM. (A) Hematopoietic progenitor cells and NK precursor cells were identified in the BM of untreated NOD/SCID mice by staining with CD34/CD38 (top panel) and CD34/CD7 (bottom panel). Cells falling into the gates R1 (CD34+CD38-: 1.5% of total BM cells), R2 (CD34+CD38+: 12%), R3 (CD34+CD7+: 0.5%), and R4 (CD34-CD7+: 1.5%) were sorted and cultured for 14 days in NK differentiation medium (see “Materials and methods”). (B) The development of CD56+ NK cells in vitro was followed by FACS analysis at the indicated time points.

In vitro differentiation of human NK cells derived from FACS sorter-purified progenitor cells of NOD/SCID mouse BM. (A) Hematopoietic progenitor cells and NK precursor cells were identified in the BM of untreated NOD/SCID mice by staining with CD34/CD38 (top panel) and CD34/CD7 (bottom panel). Cells falling into the gates R1 (CD34+CD38-: 1.5% of total BM cells), R2 (CD34+CD38+: 12%), R3 (CD34+CD7+: 0.5%), and R4 (CD34-CD7+: 1.5%) were sorted and cultured for 14 days in NK differentiation medium (see “Materials and methods”). (B) The development of CD56+ NK cells in vitro was followed by FACS analysis at the indicated time points.

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