Figure 4
Figure 4. Signaling analyses in the CD34+ and CD34− compartment of MPN patients based on mutant JAK2 status. (A) Bar charts of phospho-ERK and phospho-STAT5 staining in CD34+ comparing control and MPN patients are shown. No significant differences in signaling are demonstrated between JAK2 wild-type MPN patients and those with mutant JAK2. (B) Signaling patterns were analyzed by mutant JAK2 status in CD34− cells. Bar graphs of ERK and STAT3 signaling are shown. A significant difference was demonstrated in both pathways by JAK2 genotype. (C) A correlation graph comparing the relationship of the JAK2 V617F mutant allele burden in Lin−/CD34+/CD38− HSCs with the phopho-STAT5 and ERK levels within is shown. The correlation is poor, suggesting that factors other than the JAK2 V617F mutant burden contribute to the signaling demonstrated in MPN patients.

Signaling analyses in the CD34+ and CD34 compartment of MPN patients based on mutant JAK2 status. (A) Bar charts of phospho-ERK and phospho-STAT5 staining in CD34+ comparing control and MPN patients are shown. No significant differences in signaling are demonstrated between JAK2 wild-type MPN patients and those with mutant JAK2. (B) Signaling patterns were analyzed by mutant JAK2 status in CD34 cells. Bar graphs of ERK and STAT3 signaling are shown. A significant difference was demonstrated in both pathways by JAK2 genotype. (C) A correlation graph comparing the relationship of the JAK2 V617F mutant allele burden in Lin/CD34+/CD38 HSCs with the phopho-STAT5 and ERK levels within is shown. The correlation is poor, suggesting that factors other than the JAK2 V617F mutant burden contribute to the signaling demonstrated in MPN patients.

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