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Role of L3T4 in antigen-driven activation of a class I-specific T cell hybridoma
The expression of L3T4/Lyt-2 on murine T cells has led to the association of these surface markers with recognition of either class II or class I major histo-compatibility complex (MHC) antigens. It has been suggested that these T cell surface antigens interact with nonpolymorphic determinants on MH...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1985
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187698/ https://www.ncbi.nlm.nih.gov/pubmed/3925069 |
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collection | PubMed |
description | The expression of L3T4/Lyt-2 on murine T cells has led to the association of these surface markers with recognition of either class II or class I major histo-compatibility complex (MHC) antigens. It has been suggested that these T cell surface antigens interact with nonpolymorphic determinants on MHC antigens. We have examined the role of L3T4 in the recognition of H-2Dd by the T cell hybridoma, 3DT52.5. Mouse L cells transfected with either the H-2Dd gene, or with both the alpha and beta genes of I-Ak and the H-2Dd gene have been used to assess the role of an L3T4/la interaction at varying doses of H-2Dd. A role of L3T4 in activation of 3DT52.5 becomes evident only at limiting doses of antigen. It appears that an L3T4/la interaction can influence T cell function during suboptimal stimulation, implying that the L3T4/la interaction serves to raise the functional affinity of interaction between the T cell and the antigen-bearing cell. |
format | Text |
id | pubmed-2187698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1985 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21876982008-04-17 Role of L3T4 in antigen-driven activation of a class I-specific T cell hybridoma J Exp Med Articles The expression of L3T4/Lyt-2 on murine T cells has led to the association of these surface markers with recognition of either class II or class I major histo-compatibility complex (MHC) antigens. It has been suggested that these T cell surface antigens interact with nonpolymorphic determinants on MHC antigens. We have examined the role of L3T4 in the recognition of H-2Dd by the T cell hybridoma, 3DT52.5. Mouse L cells transfected with either the H-2Dd gene, or with both the alpha and beta genes of I-Ak and the H-2Dd gene have been used to assess the role of an L3T4/la interaction at varying doses of H-2Dd. A role of L3T4 in activation of 3DT52.5 becomes evident only at limiting doses of antigen. It appears that an L3T4/la interaction can influence T cell function during suboptimal stimulation, implying that the L3T4/la interaction serves to raise the functional affinity of interaction between the T cell and the antigen-bearing cell. The Rockefeller University Press 1985-07-01 /pmc/articles/PMC2187698/ /pubmed/3925069 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 Role of L3T4 in antigen-driven activation of a class I-specific T cell hybridoma |
title | Role of L3T4 in antigen-driven activation of a class I-specific T cell hybridoma |
title_full | Role of L3T4 in antigen-driven activation of a class I-specific T cell hybridoma |
title_fullStr | Role of L3T4 in antigen-driven activation of a class I-specific T cell hybridoma |
title_full_unstemmed | Role of L3T4 in antigen-driven activation of a class I-specific T cell hybridoma |
title_short | Role of L3T4 in antigen-driven activation of a class I-specific T cell hybridoma |
title_sort | role of l3t4 in antigen-driven activation of a class i-specific t cell hybridoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187698/ https://www.ncbi.nlm.nih.gov/pubmed/3925069 |