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Molecular and Cellular Biology, March 1999, p. 2416-2424, Vol. 19, No. 3
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Shp-2 Tyrosine Phosphatase Functions as a Negative
Regulator of the Interferon-Stimulated Jak/STAT Pathway
Min
You,
De-Hua
Yu, and
Gen-Sheng
Feng*
Department of Biochemistry and Molecular
Biology, Walther Oncology Center, Indiana University School of
Medicine, Indianapolis, Indiana 46202-5254, and Walther Cancer
Institute, Indianapolis, Indiana 46208
Received 6 August 1998/Returned for modification 15 September
1998/Accepted 18 November 1998
Shp-2 is an SH2 domain-containing protein tyrosine phosphatase.
Although the mechanism remains to be defined, substantial experimental
data suggest that Shp-2 is primarily a positive regulator in cell
growth and development. We present evidence here that Shp-2, while
acting to promote mitogenic signals, also functions as a negative
effector in interferon (IFN)-induced growth-inhibitory and apoptotic
pathways. Treatment of mouse fibroblast cells lacking a functional
Shp-2 with IFN-
or IFN-
resulted in an augmented suppression of
cell viability compared to that of wild-type cells. To dissect the
molecular mechanism, we examined IFN-induced activation of signal
transducers and activators of transcription (STATs) by electrophoretic
mobility shift assay, using a specific DNA probe (hSIE). The amounts of
STAT proteins bound to hSIE upon IFN-
or IFN-
stimulation were
significantly increased in Shp-2
/
cells. Consistently,
tyrosine phosphorylation levels of Stat1 upon IFN-
treatment and, to
a lesser extent, upon IFN-
stimulation were markedly elevated in
mutant cells. Furthermore, IFN-
induced a higher level of caspase 1 expression in Shp-2
/
cells than in wild-type cells.
Reintroduction of wild-type Shp-2 protein reversed the hypersensitivity
of Shp-2
/
fibroblasts to the cytotoxic effect of
IFN-
and IFN-
. Excessive activation of STATs by IFNs was also
diminished in mutant cells in which Shp-2 had been reintroduced.
Together, these results establish that Shp-2 functions as a negative
regulator of the Jak/STAT pathway. We propose that Shp-2 acts to
promote cell growth and survival through two mechanisms, i.e., the
stimulation of growth factor-initiated mitogenic pathways and the
suppression of cytotoxic effect elicited by cytokines, such as IFNs.
*
Corresponding author. Mailing address: Walther Oncology
Center, Indiana University School of Medicine, 1044 W. Walnut St., Room
302, Indianapolis, IN 46202-5254. Phone: (317) 274-7515. Fax: (317)
274-7592. E-mail: gfeng{at}iupui.edu.
Molecular and Cellular Biology, March 1999, p. 2416-2424, Vol. 19, No. 3
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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