MEK kinase 1 activity is required for definitive erythropoiesis in the mouse fetal liver

Abstract

AbstractMitogen-activated protein kinase/extracellular signal to regulated kinase (MEK) kinase 1 (MEKK1) is a c-Jun N-terminal kinase (JNK) activating kinase known to be implicated in proinflammatory responses and cell motility. Using mice deficient for MEKK1 kinase activity (Mekk1ΔKD) we show a role for MEKK1 in definitive mouse erythropoiesis. Although Mekk1ΔKD mice are alive and fertile on a 129 × C57/BL6 background, the frequency of Mekk1ΔKD embryos that develop past embryonic day (E) 14.5 is dramatically reduced when backcrossed into the C57/BL6 background. At E13.5, Mekk1ΔKD embryos have normal morphology but are anemic due to failure of definitive erythropoiesis. When Mekk1ΔKD fetal liver cells were transferred to lethally irradiated wild-type hosts, mature red blood cells were generated from the mutant cells, suggesting that MEKK1 functions in a non–cell-autonomous manner. Based on immunohistochemical and hemoglobin chain transcription analysis, we propose that the failure of definitive erythropoiesis is due to a deficiency in enucleation activity caused by insufficient macrophage-mediated nuclear DNA destruction.