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

Research output: Contribution to journalJournal articleResearchpeer-review

Mitogen-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 (Mekk1(DeltaKD)) we show a role for MEKK1 in definitive mouse erythropoiesis. Although Mekk1(DeltaKD) mice are alive and fertile on a 129 x C57/BL6 background, the frequency of Mekk1(DeltaKD) embryos that develop past embryonic day (E) 14.5 is dramatically reduced when backcrossed into the C57/BL6 background. At E13.5, Mekk1(DeltaKD) embryos have normal morphology but are anemic due to failure of definitive erythropoiesis. When Mekk1(DeltaKD) 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.
Original languageEnglish
Issue number10
Pages (from-to)3396-404
Number of pages8
Publication statusPublished - 2005

Bibliographical note

Keywords: Animals; Cell Nucleus; DNA; Embryo, Mammalian; Erythropoiesis; Hematopoiesis, Extramedullary; Hemoglobins; Liver; Liver Transplantation; MAP Kinase Kinase Kinase 1; Macrophages; Mice; Mice, Knockout

ID: 8441600