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Blood, 1 March 2001, Vol. 97, No. 5, pp. 1298-1305
HEMATOPOIESIS
Early growth response gene 1 stimulates development of
hematopoietic progenitor cells along the macrophage lineage at the
expense of the granulocyte and erythroid lineages
Kandasamy Krishnaraju,
Barbara Hoffman, and
Dan A. Liebermann
From the Fels Institute for Cancer Research and
Molecular Biology and the Department of Biochemistry, Temple
University School of Medicine, Philadelphia, PA.
Using a variety of differentiation-inducible myeloid cell lines, we
previously showed that the zinc-finger transcription factor early
growth response gene 1 (Egr-1) is a positive modulator of macrophage
differentiation and negatively regulates granulocytic differentiation.
In this study, high-efficiency retroviral transduction was used to
ectopically express Egr-1 in myeloid-enriched or stem cell-enriched
bone marrow cultures to explore its effect on the development of
hematopoietic progenitors in vitro and in lethally irradiated mice. It
was found that ectopic Egr-1 expression in normal hematopoietic
progenitors stimulates development along the macrophage lineage at the
expense of development along the granulocyte or erythroid lineages,
regardless of the cytokine used. Moreover, Egr-1 accelerated macrophage
development by suppressing the proliferative phase of the
growth-to-macrophage developmental program. The remarkable ability of
Egr-1 to dictate macrophage development at the expense of development
along other lineages resulted in failure of Egr-1-infected
hematopoietic progenitors to repopulate the bone marrow and spleen, and
thereby prevent death, in lethally irradiated mice. These observations
further highlight the role Egr-1 plays in monocytic
differentiation and growth suppression.

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