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      Jak2 deficiency defines an essential developmental checkpoint in definitive hematopoiesis.

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      Anemia, Animals, B-Lymphocytes, cytology, Cytokines, pharmacology, DNA-Binding Proteins, genetics, Erythrocytes, Erythroid Precursor Cells, Fibroblasts, Hematopoiesis, Hematopoietic Stem Cells, Interferon Regulatory Factor-1, Janus Kinase 2, Leukopoiesis, Liver, embryology, Mice, Mice, Knockout, Phenotype, Phosphoproteins, Protein-Tyrosine Kinases, physiology, Proto-Oncogene Proteins, RNA, Messenger, analysis, Receptors, Cytokine, Receptors, Erythropoietin

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          Abstract

          Janus kinases (Jaks) play an important role in signal transduction via cytokine and growth factor receptors. A targeted inactivation of Jak2 was performed. Jak2-/- embryos are anemic and die around day 12.5 postcoitum. Primitive erythrocytes are found, but definitive erythropoiesis is absent. Compared to erythropoietin receptor-deficient mice, the phenotype of Jak2 deficiency is more severe. Fetal liver BFU-E and CFU-E colonies are completely absent. However, multilineage hematopoietic stem cells (CD34low, c-kit(pos)) can be found, and B lymphopoiesis appears intact. In contrast to IFNalpha stimulation, Jak2-/- cells do not respond to IFNgamma. Jak2-/- embryonic stem cells are competent for LIF signaling. The data provided demonstrate that Jak2 has pivotal functions for signal transduction of a set of cytokine receptors required in definitive erythropoiesis.

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