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(Received for publication, June 11, 1996)
From the Third Department of Internal Medicine, Faculty of
Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku,
Tokyo 113, Japan
Leukocyte tyrosine kinase (LTK) is a receptor
tyrosine kinase, which belongs to the insulin receptor family and is
mainly expressed in pre-B cells and brain. In this study, we show that
LTK utilizes insulin receptor substrate-1 (IRS-1) and Shc as major two
substrates and possesses two NPXY motifs for them
separately, tyrosine 485 of one NPXY motif at the
juxtamembrane domain for IRS-1 and tyrosine 862 of another
NPXY motif at the carboxyl-terminal domain for Shc. By
using Ba/F3 cells expressing epidermal growth factor receptor-LTK
chimeric receptors containing a mutation at each NPXY site,
we showed that while both NPXY motifs equally contribute to
activation of the Ras pathway and generation of mitogenic signals, only
tyrosine 485 of LTK transmits cell survival signals. These data suggest
that IRS-1 possesses anti-apoptotic function at least in LTK signaling.
Moreover, our data indicate that the survival signaling pathway of LTK
is distinct from the Ras pathway and the p70S6 kinase
pathway. Our results provide a useful insight in understanding the
distinctive roles of Shc and IRS-1 in the signal transduction system of
the insulin receptor family, and this anti-apoptotic function of IRS-1
may explain the survival effects of insulin, IGF-1, and interleukin
4.
Volume 271, Number 44,
Issue of November 1, 1996
pp. 27707-27714
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
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