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Mouse embryos lacking the receptor tyrosine kinase, Flk1, die without mature endothelial and hematopoietic cells. To investigate the role of Flk1 during vasculogenesis and hematopoiesis, we examined the developmental potential of Flk1-/- embryonic stem cells in chimeras. We show that Flk1 is required cell autonomously for endothelial development. Furthermore, Flk1-/- cells do not contribute to primitive hematopoiesis in chimeric yolk sacs or definitive hematopoiesis in adult chimeras and chimeric fetal livers. We also demonstrate that cells lacking Flk1 are unable to reach the correct location to form blood islands, suggesting that Flk1 is involved in the movement of cells from the posterior primitive streak to the yolk sac and, possibly, to the intraembryonic sites of early hematopoiesis.

Original publication

DOI

10.1016/s0092-8674(00)80283-4

Type

Journal article

Journal

Cell

Publication Date

13/06/1997

Volume

89

Pages

981 - 990

Keywords

Amnion, Animals, Blood Vessels, Cell Lineage, Chimera, Embryo, Mammalian, Embryonic and Fetal Development, Endothelium, Vascular, Hematopoiesis, Heterozygote, Homozygote, Liver, Mice, Mice, Mutant Strains, Mutagenesis, Receptor Protein-Tyrosine Kinases, Receptors, Growth Factor, Receptors, Mitogen, Receptors, Vascular Endothelial Growth Factor, Stem Cells, Yolk Sac