Fig. 6.
Fig. 6. NK cell progenitor cloning frequency decreases with exogenously added G-CSF. CD34+/Lin−/DR− cells from unprimed marrow were plated in 96-well plates in limiting dilution. The absolute cloning frequency of primitive progenitors plated without G-CSF was 0.22% ± .07%. With progenitors derived from the same donor, CD34+/Lin−/DR− cells were analyzed in LDA with G-CSF (10 ng/mL) added only once at culture initiation or at each weekly half-media change. G-CSF significantly decreased the cloning frequency of the starting population compared with that determined in the absence of G-CSF (n = 3 for all conditions, *P ≤ .001).

NK cell progenitor cloning frequency decreases with exogenously added G-CSF. CD34+/Lin/DR cells from unprimed marrow were plated in 96-well plates in limiting dilution. The absolute cloning frequency of primitive progenitors plated without G-CSF was 0.22% ± .07%. With progenitors derived from the same donor, CD34+/Lin/DR cells were analyzed in LDA with G-CSF (10 ng/mL) added only once at culture initiation or at each weekly half-media change. G-CSF significantly decreased the cloning frequency of the starting population compared with that determined in the absence of G-CSF (n = 3 for all conditions, *P ≤ .001).

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