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The first lineage commitment step of hematopoietic stem cells (HSC) results in separation into distinct lymphoid and myeloid differentiation pathways, reflected in the generation of common lymphoid and myeloid progenitors (CLP and CMP, respectively). In this report we present the first evidence for a nonredundant regulator of this process, in that adult mice deficient in expression of the flt3 ligand (FL) have severely (10-fold) reduced levels of the CLP, accompanied by reductions in the earliest identifiable B and T cell progenitors. In contrast, CMP and HSC are unaffected in FL-deficient mice. Noteworthy, CLP express high levels of both the flt3 receptor and ligand, indicating a potential autocrine role of FL in regulation of the earliest lymphoid commitment step from HSC.

Original publication




Journal article



Publication Date





463 - 472


Animals, Hematopoietic Stem Cells, Ligands, Lymphopoiesis, Membrane Proteins, Mice, Mice, Inbred C57BL, Mice, Knockout, Myelopoiesis, Phenotype, Recombinant Proteins, Stem Cell Factor