Document Detail


Stimulation of the T-cell antigen receptor-CD3 complex signaling pathway by the tyrosine phosphatase inhibitor pervanadate is mediated by inhibition of CD45: evidence for two interconnected Lck/Fyn- or zap-70-dependent signaling pathways.
MedLine Citation:
PMID:  8734787     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The tyrosine phosphatase specific inhibitor pervanadate is a potent activator of T lymphocytes through induction of tyrosine phosphorylation and downstream events of the activation cascade. Using CD45- or CD3-negative variants of the Jurkat leukemic T-cell line we show that the different biochemical events induced by pervanadate appeared to be dependent on the presence at the cell surface of either CD45 or CD3. CD45-dependent events such as tyrosine phosphorylation of Shc, activation of nuclear factor-kappa B (NF-kappa B), activator protein-1 (AP-1), transcription factors, and stimulation of interleukin-2 (IL-2) promoter and of CD69 and CD25 surface expression paralleled activation of the tyrosine kinases lck and fyn. By contrast, stimulation of calcium influx, a CD3-dependent event, paralleled zap-70 activation. The data demonstrate that the T-cell antigen receptor-CD3 (TcR-CD3) complex is functionally linked to two different protein tyrosine kinase (PTK) modules with separate specific functions and that CD45 may be an important regulator of this coupling.
Authors:
V Imbert; D Farahifar; P Auberger; D Mary; B Rossi; J F Peyron
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of inflammation     Volume:  46     ISSN:  1078-7852     ISO Abbreviation:  J. Inflamm.     Publication Date:  1996  
Date Detail:
Created Date:  1996-10-10     Completed Date:  1996-10-10     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  9511967     Medline TA:  J Inflamm     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  65-77     Citation Subset:  IM    
Affiliation:
INSERM Unité 364, Faculté de Médecine Pasteur, Nice, France.
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MeSH Terms
Descriptor/Qualifier:
Antigens, CD3 / immunology*
Antigens, CD45 / immunology*
Base Sequence
Binding Sites
DNA / chemistry,  metabolism
Enzyme Inhibitors / pharmacology
Humans
Interleukin-2 / genetics
Lymphocyte Specific Protein Tyrosine Kinase p56(lck)
Molecular Sequence Data
Promoter Regions, Genetic
Protein Tyrosine Phosphatases / antagonists & inhibitors*
Protein-Tyrosine Kinases / metabolism
Receptors, Antigen, T-Cell / immunology*
Signal Transduction / drug effects*
T-Lymphocytes / immunology
Transcription Factors / metabolism
Tumor Cells, Cultured
Vanadates / pharmacology*
ZAP-70 Protein-Tyrosine Kinase
src-Family Kinases / metabolism
Chemical
Reg. No./Substance:
0/Antigens, CD3; 0/Enzyme Inhibitors; 0/Interleukin-2; 0/Receptors, Antigen, T-Cell; 0/Transcription Factors; 0/Vanadates; 0/pervanadate; 9007-49-2/DNA; EC 2.7.1.112/ZAP70 protein, human; EC 2.7.10.1/Protein-Tyrosine Kinases; EC 2.7.10.2/Lymphocyte Specific Protein Tyrosine Kinase p56(lck); EC 2.7.10.2/ZAP-70 Protein-Tyrosine Kinase; EC 2.7.10.2/src-Family Kinases; EC 3.1.3.48/Antigens, CD45; EC 3.1.3.48/Protein Tyrosine Phosphatases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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