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Prepublished online as a Blood First Edition Paper on October 31, 2002; DOI 10.1182/blood-2002-06-1862.
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Blood, 1 March 2003, Vol. 101, No. 5, pp. 1784-1789
HEMATOPOIESIS
Combined effects of Notch signaling and cytokines
induce a multiple log increase in precursors with lymphoid and myeloid
reconstituting ability
Barbara Varnum-Finney,
Carolyn Brashem-Stein, and
Irwin D. Bernstein
From the Clinical Research Division, Fred Hutchinson
Cancer Research Center, Seattle, WA; and the Department of Pediatrics,
University of Washington, Seattle.
We investigated whether combined signaling induced by engineered
Notch ligands and hematopoietic growth factors influences hematopoietic
stem-cell differentiation. We show that incubation of murine marrow
precursors with Delta1ext-IgG, a Notch ligand
consisting of the Delta1 extracellular domain fused to the Fc
portion of human immunoglobulin G1 (IgG1), and growth factors
stem cell factor (SCF), interleukin 6 (IL-6), IL-11, and Flt3-l
inhibited myeloid differentiation and promoted a several-log increase
in the number of precursors capable of short-term lymphoid and myeloid
repopulation. Addition of IL7 promoted early T-cell development,
whereas addition of granulocyte-macrophage colony-stimulating factor
(GM-CSF) led to terminal myeloid differentiation. These results
support a role for combinatorial effects by Notch and cytokine-induced signaling pathways in regulating hematopoietic cell
fate and suggest the usefulness of Notch ligand in increasing hematopoietic precursor numbers for clinical stem-cell transplantation.

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