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PMID: 9506979 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The Src and signal transducers and activators of transcription pathways as specific targets for low molecular weight phosphotyrosine-protein phosphatase in platelet-derived growth factor signaling.

The Journal of biological chemistry ·Vol. 273 ·No. 12 ·1998-03-20 ·Pages 6776-85

Chiarugi P, Cirri P, Marra F, Raugei G, Fiaschi T, Camici G, Manao G, Romanelli RG, Ramponi G

Abstract

The low molecular weight phosphotyrosine-protein phosphatase (LMW-PTP) is a cytosolic phosphotyrosine-protein phosphatase specifically interacting with the activated platelet-derived growth factor (PDGF) receptor through its active site. Overexpression of the LMW-PTP results in modulation of PDGF-dependent mitogenesis. In this study we investigated the effects of this tyrosine phosphatase on the signaling pathways relevant for PDGF-dependent DNA synthesis. NIH 3T3 cells were stably transfected with active or dominant negative LMW-PTP. The effects of LMW-PTP were essentially restricted to the G1 phase of the cell cycle. Upon stimulation with PDGF, cells transfected with the dominant negative LMW-PTP showed an increased activation of Src, whereas the active LMW-PTP induced a reduced activation of this proto-oncogene. We observe that c-Src binding to PDGF receptor upon stimulation is prevented by overexpression of LMW-PTP. These effects were associated with parallel changes in myc expression. Moreover, wild-type and dominant negative LMW-PTP differentially regulated STAT1 and STAT3 activation and tyrosine phosphorylation, whereas they did not modify extracellular signal-regulated kinase activity. However, these modifications were associated with changes in fos expression despite the lack of any effect on extracellular signal-regulated kinase activation. Other independent pathways involved in PDGF-induced mitogenesis, such as phosphatidylinositol 3-kinase and phospholipase C-gamma1, were not affected by LMW-PTP. These data indicate that this phosphatase selectively interferes with the Src and the STATs pathways in PDGF downstream signaling. The resulting changes in myc and fos proto-oncogene expression are likely to mediate the modifications observed in the G1 phase of the cell cycle.

MeSH Terms
3T3 Cells Animals Chemotaxis DNA-Binding Proteins/metabolism G1 Phase Mice Molecular Weight Oncogene Protein pp60(v-src)/metabolism Platelet-Derived Growth Factor/metabolism Protein Tyrosine Phosphatases/chemistry,metabolism Proto-Oncogene Proteins c-myc/metabolism Receptors, Platelet-Derived Growth Factor/metabolism STAT1 Transcription Factor STAT3 Transcription Factor Signal Transduction Trans-Activators/metabolism Transcription, Genetic
Chemicals
DNA-Binding Proteins Platelet-Derived Growth Factor Proto-Oncogene Proteins c-myc STAT1 Transcription Factor STAT3 Transcription Factor Stat1 protein, mouse Stat3 protein, mouse Trans-Activators Receptors, Platelet-Derived Growth Factor Oncogene Protein pp60(v-src) Protein Tyrosine Phosphatases
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Chiarugi P
Dipartimento di Scienze Biochimiche, viale Morgagni 50, 50134 Firenze, Italy.
Cirri P
Marra F
Raugei G
Fiaschi T
Camici G
Manao G
Romanelli R G
Ramponi G
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1998-03-20
Pages
6776-85
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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