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Itk and Fyn Make Independent Contributions to T Cell Activation

Itk is a member of the Btk/Tec/Itk family of nonreceptor protein tyrosine kinases (PTKs), and has been implicated in T cell antigen receptor (TCR) signal transduction. Lck and Fyn are the Src-family nonreceptor PTKs that are involved in TCR signaling. To address the question of how these members of...

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Detalles Bibliográficos
Autores principales: Liao, X. Charlene, Littman, Dan R., Weiss, Arthur
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2199174/
https://www.ncbi.nlm.nih.gov/pubmed/9396778
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author Liao, X. Charlene
Littman, Dan R.
Weiss, Arthur
author_facet Liao, X. Charlene
Littman, Dan R.
Weiss, Arthur
author_sort Liao, X. Charlene
collection PubMed
description Itk is a member of the Btk/Tec/Itk family of nonreceptor protein tyrosine kinases (PTKs), and has been implicated in T cell antigen receptor (TCR) signal transduction. Lck and Fyn are the Src-family nonreceptor PTKs that are involved in TCR signaling. To address the question of how these members of different families of PTKs functionally contribute to T cell development and to T cell activation, mice deficient for both Itk and either Lck or Fyn were generated. The Itk/Lck doubly deficient mice exhibited a phenotype similar to that of Lck-deficient mice. The phenotype of the Itk/Fyn doubly deficient mice was similar to that of Itk deficient mice. However the Itk/Fyn doubly deficient mice exhibited a more severe defect in TCR-induced proliferation of thymocytes and peripheral T cells than did mice deficient in either kinase alone. These data support the notion that Itk and Fyn both make independent contributions to TCR-induced T cell activation.
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spelling pubmed-21991742008-04-16 Itk and Fyn Make Independent Contributions to T Cell Activation Liao, X. Charlene Littman, Dan R. Weiss, Arthur J Exp Med Brief Definitive Report Itk is a member of the Btk/Tec/Itk family of nonreceptor protein tyrosine kinases (PTKs), and has been implicated in T cell antigen receptor (TCR) signal transduction. Lck and Fyn are the Src-family nonreceptor PTKs that are involved in TCR signaling. To address the question of how these members of different families of PTKs functionally contribute to T cell development and to T cell activation, mice deficient for both Itk and either Lck or Fyn were generated. The Itk/Lck doubly deficient mice exhibited a phenotype similar to that of Lck-deficient mice. The phenotype of the Itk/Fyn doubly deficient mice was similar to that of Itk deficient mice. However the Itk/Fyn doubly deficient mice exhibited a more severe defect in TCR-induced proliferation of thymocytes and peripheral T cells than did mice deficient in either kinase alone. These data support the notion that Itk and Fyn both make independent contributions to TCR-induced T cell activation. The Rockefeller University Press 1997-12-15 /pmc/articles/PMC2199174/ /pubmed/9396778 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Brief Definitive Report
Liao, X. Charlene
Littman, Dan R.
Weiss, Arthur
Itk and Fyn Make Independent Contributions to T Cell Activation
title Itk and Fyn Make Independent Contributions to T Cell Activation
title_full Itk and Fyn Make Independent Contributions to T Cell Activation
title_fullStr Itk and Fyn Make Independent Contributions to T Cell Activation
title_full_unstemmed Itk and Fyn Make Independent Contributions to T Cell Activation
title_short Itk and Fyn Make Independent Contributions to T Cell Activation
title_sort itk and fyn make independent contributions to t cell activation
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2199174/
https://www.ncbi.nlm.nih.gov/pubmed/9396778
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