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. 2005 May 2;201(9):1421–1433. doi: 10.1084/jem.20042294

Figure 2.

Figure 2.

In vitro expansion of NK cells. (A) CD45−/− and control NK1.1+CD49b+TCR-β cells were sorted and cultured in various concentrations of IL-15 for 60 h. Cultures were pulsed with [3H]thymidine for the final 8 h and radioactive incorporation counted. (B) CD45−/− and control NK1.1+CD49b+TCR-β cells were cultured for 48 or 72 h in 50 ng/ml IL-15 with or without 100 ng/ml IL-21. Cultures were pulsed with [3H]thymidine for the final 8 h and radio-labeled DNA counted. For A and B data are representative of four independent experiments. (C) Cells cultured in IL-15 with or without IL-21 for 72 h were analyzed for surface expression levels of NK1.1 by flow cytometry. Data are representative of three independent experiments.