Fig. 5.
Fig. 5. EE-T-Y343 and EE-T-Y343F retain high capacities to cosignal in combination with c-Kit. / Erythroid progenitor cells were prepared from TAP-treated mice at 70 hours after TAP withdrawal (c-Kit+, EPO receptor+, Ter119− stage) and were used in proliferation response assays to assess the abilities of these minimal EPO receptor forms to cosignal with endogenous c-Kit. Specifically, cells at 5 × 106 cells per milliliter were exposed to EPO, hEGF, or SCF at the concentration indexed, and proliferation was assayed based on rates of cytokine-induced methyl–[3H]-thymidine ([3H]dT) incorporation. Stem cell factor (+SCF) was included at a concentration of 50 ng/mL (50% or lower maximum dose as shown in parallel and independent SCF-only response profiles).

EE-T-Y343 and EE-T-Y343F retain high capacities to cosignal in combination with c-Kit.

Erythroid progenitor cells were prepared from TAP-treated mice at 70 hours after TAP withdrawal (c-Kit+, EPO receptor+, Ter119 stage) and were used in proliferation response assays to assess the abilities of these minimal EPO receptor forms to cosignal with endogenous c-Kit. Specifically, cells at 5 × 106 cells per milliliter were exposed to EPO, hEGF, or SCF at the concentration indexed, and proliferation was assayed based on rates of cytokine-induced methyl–[3H]-thymidine ([3H]dT) incorporation. Stem cell factor (+SCF) was included at a concentration of 50 ng/mL (50% or lower maximum dose as shown in parallel and independent SCF-only response profiles).

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