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Blood, 1 March 2008, Vol. 111, No. 5, pp. 2636-2639. Prepublished online as a Blood First Edition Paper on January 3, 2008; DOI 10.1182/blood-2007-11-124685.
Submitted November 19, 2007
Center for Pediatric Biomedical Research, University of Rochester Medical Center, Rochester, NY, United States * Corresponding author; email: james_palis{at}urmc.rochester.edu.
Hematopoiesis initiates within the yolk sac of mammalian embryos in overlapping primitive and definitive waves each containing erythroid and megakaryocyte lineages. c-myb-null mouse fetuses lack definitive erythrocytes but contain circulating primitive erythroblasts and hepatic megakaryocytes. However, it is unclear if c-myb-null embryos harbor definitive erythroid or megakaryocyte progenitors. We determined that c-myb is not expressed in primitive erythroid precursors and that c-myb-null embryos have normal primitive erythroid and megakaryocyte progenitor numbers and kinetics between E7.0-E9.0. While primitive hematopoiesis is c-myb-independent, no definitive erythroid potential was detected in c-myb-null embryos, confirming that definitive erythropoiesis, beginning at E8.25 in the yolk sac, is completely c-myb-dependent. In contrast, reduced numbers of megakaryocyte progenitors with restricted proliferative capacity persist in E10.5 yolk sac and E11.5 liver. Despite this impaired megakaryocyte potential, c-myb-null fetuses have normal platelet numbers at E12.5 but became thrombocytopenic by E15.5, suggesting that c-myb is required for sustained thrombopoiesis.
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