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Volume 272, Number 29,
Issue of July 18, 1997
pp. 18026-18032
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.
Characterization of a Novel
Na+-dependent, Guanosine-specific,
Nitrobenzylthioinosine-sensitive Transporter in Acute Promyelocytic
Leukemia Cells
(Received for publication, March 20, 1997, and in revised form, May 13, 1997)
Sheryl A.
Flanagan
and
Kelly A.
Meckling-Gill
From the Department of Human Biology and Nutritional Sciences,
University of Guelph, Guelph, Ontario N1G 2W1, Canada
NB4 cells are the only bona fide in
vitro model of human acute promyelocytic leukemia. We have
examined cytidine and guanosine transport in this cell line and
characterized a novel guanosine-specific transporter. Cytidine
transport occurred predominately by equilibrative nitrobenzylthioinosine (NBMPR)-sensitive (es) transport. In
the presence of Na+, guanosine at various concentrations
accumulated at least 6-fold above equilibrium. The initial rate of
guanosine transport in Na+ buffer decreased by 75% with
the addition of 1 µM NBMPR and the IC50 for
NBMPR inhibition was 0.7 ± 0.1 nM. Replacement of
Na+ with choline also resulted in a 75% decrease in total
guanosine transport. The potent inhibition of guanosine transport by
NBMPR and the loss of transport in choline suggested that a
Na+-dependent NBMPR-sensitive transporter was
responsible for the majority of guanosine uptake. This concentrative,
sensitive transporter is Na+ dependent with a
stoichiometric coupling ratio of 1:1. This novel transporter, referred
to as csg, is guanosine-specific with total guanosine
transport inhibited by only 50% in the presence of 1 mM
competing nucleosides. HL-60, acute myelocytic leukemia cells, do not
exhibit csg activity while L1210, murine acute lymphocytic leukemia cells, exhibit csg transport. The presence of the
csg transporter suggests an important role for guanosine in
particular forms of leukemia and may provide a new target for cytotoxic
therapy.

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Copyright © 1997 by the American Society for Biochemistry and Molecular Biology.
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