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Unc119, a Novel Activator of Lck/Fyn, Is Essential for T Cell Activation

The first step in T cell receptor for antigen (TCR) signaling is the activation of the receptor-bound Src kinases, Lck and Fyn. The exact mechanism of this process is unknown. Here, we report that the novel Src homology (SH) 3/SH2 ligand–Uncoordinated 119 (Unc119) associates with CD3 and CD4, and ac...

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Detalles Bibliográficos
Autores principales: Gorska, Magdalena M., Stafford, Susan J., Cen, Osman, Sur, Sanjiv, Alam, Rafeul
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211793/
https://www.ncbi.nlm.nih.gov/pubmed/14757743
http://dx.doi.org/10.1084/jem.20030589
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author Gorska, Magdalena M.
Stafford, Susan J.
Cen, Osman
Sur, Sanjiv
Alam, Rafeul
author_facet Gorska, Magdalena M.
Stafford, Susan J.
Cen, Osman
Sur, Sanjiv
Alam, Rafeul
author_sort Gorska, Magdalena M.
collection PubMed
description The first step in T cell receptor for antigen (TCR) signaling is the activation of the receptor-bound Src kinases, Lck and Fyn. The exact mechanism of this process is unknown. Here, we report that the novel Src homology (SH) 3/SH2 ligand–Uncoordinated 119 (Unc119) associates with CD3 and CD4, and activates Lck and Fyn. Unc119 overexpression increases Lck/Fyn activity in T cells. In Unc119-deficient T cells, Lck/Fyn activity is dramatically reduced with concomitant decrease in interleukin 2 production and cellular proliferation. Reconstitution of cells with Unc119 reverses the signaling and functional outcome. Thus, Unc119 is a receptor-associated activator of Src-type kinases. It provides a novel mechanism of signal generation in the TCR complex.
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spelling pubmed-22117932008-03-11 Unc119, a Novel Activator of Lck/Fyn, Is Essential for T Cell Activation Gorska, Magdalena M. Stafford, Susan J. Cen, Osman Sur, Sanjiv Alam, Rafeul J Exp Med Article The first step in T cell receptor for antigen (TCR) signaling is the activation of the receptor-bound Src kinases, Lck and Fyn. The exact mechanism of this process is unknown. Here, we report that the novel Src homology (SH) 3/SH2 ligand–Uncoordinated 119 (Unc119) associates with CD3 and CD4, and activates Lck and Fyn. Unc119 overexpression increases Lck/Fyn activity in T cells. In Unc119-deficient T cells, Lck/Fyn activity is dramatically reduced with concomitant decrease in interleukin 2 production and cellular proliferation. Reconstitution of cells with Unc119 reverses the signaling and functional outcome. Thus, Unc119 is a receptor-associated activator of Src-type kinases. It provides a novel mechanism of signal generation in the TCR complex. The Rockefeller University Press 2004-02-02 /pmc/articles/PMC2211793/ /pubmed/14757743 http://dx.doi.org/10.1084/jem.20030589 Text en Copyright © 2004, The Rockefeller University Press 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 Article
Gorska, Magdalena M.
Stafford, Susan J.
Cen, Osman
Sur, Sanjiv
Alam, Rafeul
Unc119, a Novel Activator of Lck/Fyn, Is Essential for T Cell Activation
title Unc119, a Novel Activator of Lck/Fyn, Is Essential for T Cell Activation
title_full Unc119, a Novel Activator of Lck/Fyn, Is Essential for T Cell Activation
title_fullStr Unc119, a Novel Activator of Lck/Fyn, Is Essential for T Cell Activation
title_full_unstemmed Unc119, a Novel Activator of Lck/Fyn, Is Essential for T Cell Activation
title_short Unc119, a Novel Activator of Lck/Fyn, Is Essential for T Cell Activation
title_sort unc119, a novel activator of lck/fyn, is essential for t cell activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211793/
https://www.ncbi.nlm.nih.gov/pubmed/14757743
http://dx.doi.org/10.1084/jem.20030589
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