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Prepublished online as a Blood First Edition Paper on October 24, 2002; DOI 10.1182/blood-2002-07-2051.
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Blood, 1 March 2003, Vol. 101, No. 5, pp. 1777-1783
HEMATOPOIESIS
HES-1 preserves purified hematopoietic stem cells ex vivo and
accumulates side population cells in vivo
Atsushi Kunisato,
Shigeru Chiba,
Etsuko Nakagami-Yamaguchi,
Keiki Kumano,
Toshiki Saito,
Shigeo Masuda,
Tomoyuki Yamaguchi,
Masatake Osawa,
Ryoichiro Kageyama,
Hiromitsu Nakauchi,
Mitsuo Nishikawa, and
Hisamaru Hirai
From the Departments of Hematology and Oncology,
Graduate School of Medicine, and Cell Therapy and Transplantation
Medicine, University of Tokyo Hospital, University of Tokyo,
Japan; the Riken Center for Developmental Biology, Kobe,
Japan; the Institute for Virus Research, Kyoto University,
Japan; the Department of Immunology, Institute of Basic
Medical Science, University of Tsukuba, Japan; and the
Kirin Brewery Pharmaceutical Research Laboratory, Takasaki,
Japan.
Mouse long-term hematopoietic reconstituting cells exist in the
c-Kit+Sca-1+Lin (KSL) cell
population; among them, CD34low/ cells represent the most
highly purified population of hematopoietic stem cells in the adult
bone marrow. Here, we demonstrate that retrovirus-mediated transduction
of
CD34low/ c-Kit+Sca-1+Lin
(34 KSL) cells with the HES-1 gene, which
encodes a basic helix-loop-helix transcription factor functioning
downstream of the Notch receptor, and is a key molecule for the growth
phase of neural stem cells in the embryo, preserves the long-term
reconstituting activity of these cells in vitro. We also show that
cells derived from the HES-1-transduced
34 KSL population produce progenies characterized by
negative Hoechst dye staining, which defines the side population, and
by CD34low/ profile in the bone marrow KSL population in
each recipient mouse at ratios 3.5- and 7.8-fold those produced by
nontransduced 34 KSL-derived competitor cells. We conclude
that HES-1 preserves the long-term reconstituting
hematopoietic activity of 34 KSL stem cells ex vivo.
Up-regulation of HES-1 protein in the 34 KSL population
before unnecessary cell division, that is, without retrovirus
transduction, may represent a potent approach to absolute expansion of
hematopoietic stem cells.

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