Figure 4
Figure 4. CD56dim NK cells proliferate less than CD56bright NK cells. Enriched NK cells were sorted into CD56bright KIR−, CD56dim KIR−, and CD56dim KIR+ NK cells and assayed for proliferation after 14 days of culture with the mouse stromal cell EL08–1D2 and exogenous IL-15 (n = 4). NK cells were either in direct contact with the stromal cells (black bars: EL Contact) or separated from them by a Transwell membrane (hatched bars: EL TW). These data are shown in the lower part of the figure: CD56bright KIR− NK cells proliferated more than either CD56dim subset (*P < .01) and the CD56dim KIR− population proliferated more than CD56dim KIR+ cells (P = .001). In the experiment shown in the boxed, upper part of the figure the CD56dim KIR− subset was further divided into CD56dim NKG2A−KIR− and NKG2A+KIR− subsets (n = 4) and tested in a 6-day thymidine incorporation assay where the NKG2A−KIR− subset showed less short-term responsiveness to IL-15 (10 ng/mL) (P = .002). Error bars indicate SEM.

CD56dim NK cells proliferate less than CD56bright NK cells. Enriched NK cells were sorted into CD56bright KIR, CD56dim KIR, and CD56dim KIR+ NK cells and assayed for proliferation after 14 days of culture with the mouse stromal cell EL08–1D2 and exogenous IL-15 (n = 4). NK cells were either in direct contact with the stromal cells (black bars: EL Contact) or separated from them by a Transwell membrane (hatched bars: EL TW). These data are shown in the lower part of the figure: CD56bright KIR NK cells proliferated more than either CD56dim subset (*P < .01) and the CD56dim KIR population proliferated more than CD56dim KIR+ cells (P = .001). In the experiment shown in the boxed, upper part of the figure the CD56dim KIR subset was further divided into CD56dim NKG2AKIR and NKG2A+KIR subsets (n = 4) and tested in a 6-day thymidine incorporation assay where the NKG2AKIR subset showed less short-term responsiveness to IL-15 (10 ng/mL) (P = .002). Error bars indicate SEM.

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