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Thymic selection of CD8+ single positive cells with a class II major histocompatibility complex-restricted receptor

We describe mice that express a transgenic T cell receptor alpha/beta (TCR-alpha/beta) specific for peptide 111-119 from influenza hemagglutinin presented by I-Ed class II major histocompatibility complex (MHC) molecules. The transgenic TCR is expressed on CD4+8- as well as CD4-8+ mature T cells eve...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191558/
https://www.ncbi.nlm.nih.gov/pubmed/8006585
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description We describe mice that express a transgenic T cell receptor alpha/beta (TCR-alpha/beta) specific for peptide 111-119 from influenza hemagglutinin presented by I-Ed class II major histocompatibility complex (MHC) molecules. The transgenic TCR is expressed on CD4+8- as well as CD4-8+ mature T cells even in mice that are deficient in rearrangement or do not express endogenous TCR-alpha genes. The CD4-8+ T cells require I-Ed class II MHC molecules for positive selection and can be activated to proliferate and to kill by I-Ed molecules presenting the relevant peptide. Full maturation of these cells, however, also requires the presence of class I MHC molecules. The results are compatible with the notion that T cell maturation requires multiple receptor-ligand interactions and establish an exception to the rule that class II-restricted TCRs are exclusively expressed by mature CD4+8- cells.
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spelling pubmed-21915582008-04-16 Thymic selection of CD8+ single positive cells with a class II major histocompatibility complex-restricted receptor J Exp Med Articles We describe mice that express a transgenic T cell receptor alpha/beta (TCR-alpha/beta) specific for peptide 111-119 from influenza hemagglutinin presented by I-Ed class II major histocompatibility complex (MHC) molecules. The transgenic TCR is expressed on CD4+8- as well as CD4-8+ mature T cells even in mice that are deficient in rearrangement or do not express endogenous TCR-alpha genes. The CD4-8+ T cells require I-Ed class II MHC molecules for positive selection and can be activated to proliferate and to kill by I-Ed molecules presenting the relevant peptide. Full maturation of these cells, however, also requires the presence of class I MHC molecules. The results are compatible with the notion that T cell maturation requires multiple receptor-ligand interactions and establish an exception to the rule that class II-restricted TCRs are exclusively expressed by mature CD4+8- cells. The Rockefeller University Press 1994-07-01 /pmc/articles/PMC2191558/ /pubmed/8006585 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 Articles
Thymic selection of CD8+ single positive cells with a class II major histocompatibility complex-restricted receptor
title Thymic selection of CD8+ single positive cells with a class II major histocompatibility complex-restricted receptor
title_full Thymic selection of CD8+ single positive cells with a class II major histocompatibility complex-restricted receptor
title_fullStr Thymic selection of CD8+ single positive cells with a class II major histocompatibility complex-restricted receptor
title_full_unstemmed Thymic selection of CD8+ single positive cells with a class II major histocompatibility complex-restricted receptor
title_short Thymic selection of CD8+ single positive cells with a class II major histocompatibility complex-restricted receptor
title_sort thymic selection of cd8+ single positive cells with a class ii major histocompatibility complex-restricted receptor
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191558/
https://www.ncbi.nlm.nih.gov/pubmed/8006585