Figure 4
Figure 4. In vitro stimulation of F36V-Mpl increases lymphoid output from multi-lymphoid progenitors. (A) Multilymphoid progenitors (CD34+CD38−Lin−CD7+) transduced with the F36V-MPL-GFP were cultured on MS5 stroma without growth factors with or without CID. Fold increase (mean, SEM) in total number and CD19+GFP+ cells relative to day 0 is shown (n = 5 experiments, in triplicate); P = .04 and .047, respectively. (B) FACS analysis of cells cultured (D29-35) as in panel A. (C) B-cell progenitors (CD34+CD19+) and B cells (CD34−CD19+) were transduced with F36V-MPL-GFP and cultured with or without CID on MS5 stroma without cytokines. (n = 3 wells/arm; mean ± SE).

In vitro stimulation of F36V-Mpl increases lymphoid output from multi-lymphoid progenitors. (A) Multilymphoid progenitors (CD34+CD38LinCD7+) transduced with the F36V-MPL-GFP were cultured on MS5 stroma without growth factors with or without CID. Fold increase (mean, SEM) in total number and CD19+GFP+ cells relative to day 0 is shown (n = 5 experiments, in triplicate); P = .04 and .047, respectively. (B) FACS analysis of cells cultured (D29-35) as in panel A. (C) B-cell progenitors (CD34+CD19+) and B cells (CD34CD19+) were transduced with F36V-MPL-GFP and cultured with or without CID on MS5 stroma without cytokines. (n = 3 wells/arm; mean ± SE).

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