Fig. 2From: Cell competition between wild-type and JAK2V617F mutant cells prevents disease relapse after stem cell transplantation in a murine model of myeloproliferative neoplasmImmune regulation associated with wild-type and JAK2V617F mutant cell competition. A A murine model of wild-type and JAK2V617F mutant cell competition established by marrow transplantations. B Differentially enriched Gene Ontology (GO) terms in mutant Lin−cKit+ HSPCs transplanted together with wildtype cells (pooled sample from 3 mice) compared to mutant HSPCs transplanted alone (pooled sample from 2 mice). P values are plotted as the negative of their logarithm. C Spleen T cells (CD3+CD4+and CD3+CD8+) and B cells (CD3−B220+), and marrow MDSCs (both CD11b+Ly6ChighLy6G− M-MDSCs and CD11b+Ly6ClowLy6G+PMN-MDSCs) in wild-type recipient of wild-type donor (“wild-type”), JAK2V617F mutant donor (“mutant”), or both wild-type and mutant donors (“wild-type + mutant”) (spleen T cells: n = 3 mice in each group; spleen B cells: n = 3–6 mice in each group; marrow MDSCs: n = 3–6 mice in each group). D Quantitative measurement of mean fluorescence intensity for PD-L1 staining on wild-type LSK cells (n = 7 mice), JAK2V617F mutant LSK cells (n = 4 mice), and JAK2V617F mutant LSK cells with co-existing wild-type cell competition (n = 9 mice). *P < 0.05Back to article page