Figure 2
HSC/Ps with c-Myc deletion are biased toward megakaryocytic differentiation at the expense of other hematopoietic lineages. (A) CMPs, CLPs, and GMPs were significantly reduced in c-Myc−/− mouse BM; however, the number of MEPs was less affected. (B) Increased percentages of CD71+ and CD41+ (arrow), 2 distinct populations of cells in BM of c-Myc−/− mice. (C) Increased percentages of both CD41+c-kit− and CD41+c-kit+ populations in c-Myc−/− BM. (D) The absolute number of Mk-Ps (Lin−Sca1−CD41+c-kit+CD9+) is significantly increased in c-Myc−/− BM (2 hind limbs), whereas the number of Ery-Ps (CD71+Ter119−) is less affected. However, the number of Ery-Bs (CD71+Ter119+) and differentiated nucleated Erys (CD71−Ter119+) is significantly reduced in c-Myc−/− BM (2 hind limbs). (E) Proliferation of CD41+ megakaryocytes is less affected, whereas the proliferation of Gr1+ granulocytes is significantly decreased in c-Myc−/− mice. (F) HSC/Ps from c-Myc−/− mice express high levels of erythrocyte and megakaryocyte-specific genes, including Gata1, Fog1, and Eklf1, but reduced lymphoid and myeloid-specific genes, such as Pu.1. The expression levels of detected genes in c-Myc−/− LSK and LK populations are shown relative to expression levels in the WT LSK cell population. The significant reduction of c-Myc levels in c-Myc−/− HSC/Ps indicates the success of the induced c-Myc deletion. Data are an average of triplicate experiments. *P < .05; **P < .01.

HSC/Ps with c-Myc deletion are biased toward megakaryocytic differentiation at the expense of other hematopoietic lineages. (A) CMPs, CLPs, and GMPs were significantly reduced in c-Myc−/− mouse BM; however, the number of MEPs was less affected. (B) Increased percentages of CD71+ and CD41+ (arrow), 2 distinct populations of cells in BM of c-Myc−/− mice. (C) Increased percentages of both CD41+c-kit and CD41+c-kit+ populations in c-Myc−/− BM. (D) The absolute number of Mk-Ps (LinSca1CD41+c-kit+CD9+) is significantly increased in c-Myc−/− BM (2 hind limbs), whereas the number of Ery-Ps (CD71+Ter119) is less affected. However, the number of Ery-Bs (CD71+Ter119+) and differentiated nucleated Erys (CD71Ter119+) is significantly reduced in c-Myc−/− BM (2 hind limbs). (E) Proliferation of CD41+ megakaryocytes is less affected, whereas the proliferation of Gr1+ granulocytes is significantly decreased in c-Myc−/− mice. (F) HSC/Ps from c-Myc−/− mice express high levels of erythrocyte and megakaryocyte-specific genes, including Gata1, Fog1, and Eklf1, but reduced lymphoid and myeloid-specific genes, such as Pu.1. The expression levels of detected genes in c-Myc−/− LSK and LK populations are shown relative to expression levels in the WT LSK cell population. The significant reduction of c-Myc levels in c-Myc−/− HSC/Ps indicates the success of the induced c-Myc deletion. Data are an average of triplicate experiments. *P < .05; **P < .01.

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