Figure 3
Differences in STAT5 signaling and MF-specific STAT3 signaling in CD34− cells from patients with MPN. (A) Representative histogram profiles of phospho-ERK (top row) and phospho-STAT5 (middle row) staining in a control and a PV patient (left and center panels, respectively). Phospho-STAT3 staining (bottom row) is shown for an MF patient and a control. The bar graph on the right shows increased STAT5 signaling in MPN patients, which reached statistical significance in PV and MF patients compared with controls. There was also a statistical significant difference in STAT5 signaling between PV and ET patients. Statistically significant STAT3 signaling compared with controls and PV occurred only with MF patients. (B) A signaling heat-map table is shown for all control and MPN CD34− samples analyzed. The patient numbers correspond to those in Figure 2B plus additional patients for whom CD34− cells were available for analysis. Where the patient is JAK2 V617F positive, we have also documented the allele burden of the CD34−/GPA+/CD71+ compartment.

Differences in STAT5 signaling and MF-specific STAT3 signaling in CD34 cells from patients with MPN. (A) Representative histogram profiles of phospho-ERK (top row) and phospho-STAT5 (middle row) staining in a control and a PV patient (left and center panels, respectively). Phospho-STAT3 staining (bottom row) is shown for an MF patient and a control. The bar graph on the right shows increased STAT5 signaling in MPN patients, which reached statistical significance in PV and MF patients compared with controls. There was also a statistical significant difference in STAT5 signaling between PV and ET patients. Statistically significant STAT3 signaling compared with controls and PV occurred only with MF patients. (B) A signaling heat-map table is shown for all control and MPN CD34 samples analyzed. The patient numbers correspond to those in Figure 2B plus additional patients for whom CD34 cells were available for analysis. Where the patient is JAK2 V617F positive, we have also documented the allele burden of the CD34/GPA+/CD71+ compartment.

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