Fig. 4.
Fig. 4. Responsiveness of CD34+CD38−MDS cells to early-acting cytokines. / CD34+CD38− cells were plated at the single-cell level as described in “Materials and methods” and cultured in 3 different cytokine combinations: a = SCF + FL; b = SCF + FL + MGDF; and c = cocktail (SCF + FL + MGDF + IL-3 + G-CSF + GM-CSF + Epo). Five normal subjects were used as controls. Wells were scored for total clones per 120 wells and for size (3-50 cells and more than 50 cells) after 11 to 13 days of incubation. No clones were observed for MDS patients 7 and 8 in response to cytokine combination “a.” In general, the clones formed from CD34+CD38−cells were too small to allow FISH analysis.

Responsiveness of CD34+CD38MDS cells to early-acting cytokines.

CD34+CD38 cells were plated at the single-cell level as described in “Materials and methods” and cultured in 3 different cytokine combinations: a = SCF + FL; b = SCF + FL + MGDF; and c = cocktail (SCF + FL + MGDF + IL-3 + G-CSF + GM-CSF + Epo). Five normal subjects were used as controls. Wells were scored for total clones per 120 wells and for size (3-50 cells and more than 50 cells) after 11 to 13 days of incubation. No clones were observed for MDS patients 7 and 8 in response to cytokine combination “a.” In general, the clones formed from CD34+CD38cells were too small to allow FISH analysis.

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