Figure 5.
Increased incorporation of glucose carbon through glycolysis and the pentose phosphate pathway in mutant JAK2–expressing HSPCs. (A) Schematic of glucose labeling and tracing in BM LSK and MEP cells. Fluorescence-activated cell sorted (FACS) LSK cells and MEPs were cultured with [U-13C6] d-glucose for 8 hours and analyzed by ion chromatography–Fourier transform mass spectrometry (IC-FTMS) to determine the fate of labeled carbon atoms derived from glucose in various downstream metabolites. (B) Bar graphs depicting the levels (μmoles per gram of protein) of glucose-derived 13C containing isotopologues of metabolites in glycolysis and pentose phosphate pathways. LSK and MEP cells were collected and pooled from 9 to 12 mice of matching genotype as 1 replicate. Data are from 2 independent experiments. Insert showing the key rate-limiting step in glycolysis in which the activity of Pfkfb enzyme potentiated activity of rate-limiting enzyme phosphofructokinase (Pfk) through generation of fructose-2,6-biphosphate (F2,6BP) from fructose-6-phosphate (F6P). 3-(3-pyridinyl)-1-(4-pyridinyl)-2-propen-1-1 (3PO) is a specific pharmacological inhibitor of Pfkfb3 isoform. (C) Pfkfb1-4 mRNA expression in MEP cells (n = 3 per genotype). (D) Pfkfb3 protein expression in BM LSK and MEP cells as measured by intracellular FACS (n = 3 per genotype). (E) Graphical representation of increased glycolysis rate-limiting step involving conversion of F6P to F1,6BP and its positive regulator PFKFB3, which can be inhibited by 3PO. All data are presented as mean ± standard error of the mean. See also supplemental Figure 6. ***P < .001. 6PG, 6-phosphogluconate; 6PGL, 6-phosphogluconolactone; ADP, adenosine 5′-diphosphate; ATP, adenosine triphosphate; DHAP, dihydroxyacetone phosphate; E4P, erythrose 4-phosphate; F6P, fructose 6-phosphate; FBP, fructose 1,6-bisphosphate; G6P, glucose 6-phosphate; PRPP, phosphoribosyl pyrophosphate; R5P, ribose 5-phosphate; Ru5P, ribulose 5-phosphate; S7P, sedoheptulose 7-phosphate; TCA, tricarboxylic acid cycle; Xu5P, xylulose 5-phosphate.

Increased incorporation of glucose carbon through glycolysis and the pentose phosphate pathway in mutant JAK2–expressing HSPCs. (A) Schematic of glucose labeling and tracing in BM LSK and MEP cells. Fluorescence-activated cell sorted (FACS) LSK cells and MEPs were cultured with [U-13C6] d-glucose for 8 hours and analyzed by ion chromatography–Fourier transform mass spectrometry (IC-FTMS) to determine the fate of labeled carbon atoms derived from glucose in various downstream metabolites. (B) Bar graphs depicting the levels (μmoles per gram of protein) of glucose-derived 13C containing isotopologues of metabolites in glycolysis and pentose phosphate pathways. LSK and MEP cells were collected and pooled from 9 to 12 mice of matching genotype as 1 replicate. Data are from 2 independent experiments. Insert showing the key rate-limiting step in glycolysis in which the activity of Pfkfb enzyme potentiated activity of rate-limiting enzyme phosphofructokinase (Pfk) through generation of fructose-2,6-biphosphate (F2,6BP) from fructose-6-phosphate (F6P). 3-(3-pyridinyl)-1-(4-pyridinyl)-2-propen-1-1 (3PO) is a specific pharmacological inhibitor of Pfkfb3 isoform. (C) Pfkfb1-4 mRNA expression in MEP cells (n = 3 per genotype). (D) Pfkfb3 protein expression in BM LSK and MEP cells as measured by intracellular FACS (n = 3 per genotype). (E) Graphical representation of increased glycolysis rate-limiting step involving conversion of F6P to F1,6BP and its positive regulator PFKFB3, which can be inhibited by 3PO. All data are presented as mean ± standard error of the mean. See also supplemental Figure 6. ***P < .001. 6PG, 6-phosphogluconate; 6PGL, 6-phosphogluconolactone; ADP, adenosine 5′-diphosphate; ATP, adenosine triphosphate; DHAP, dihydroxyacetone phosphate; E4P, erythrose 4-phosphate; F6P, fructose 6-phosphate; FBP, fructose 1,6-bisphosphate; G6P, glucose 6-phosphate; PRPP, phosphoribosyl pyrophosphate; R5P, ribose 5-phosphate; Ru5P, ribulose 5-phosphate; S7P, sedoheptulose 7-phosphate; TCA, tricarboxylic acid cycle; Xu5P, xylulose 5-phosphate.

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