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Activated human T lymphocytes express MHC class I heavy chains not associated with beta 2-microglobulin
We present here the molecular characterization of a new activation- induced surface structure on human T lymphocytes, termed LA45, with high homology (93% at protein level) to MHC class I molecules. Antigen modulation and sequential immunoprecipitation experiments revealed that LA45 and HLA class I...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1990
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187879/ https://www.ncbi.nlm.nih.gov/pubmed/2139695 |
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collection | PubMed |
description | We present here the molecular characterization of a new activation- induced surface structure on human T lymphocytes, termed LA45, with high homology (93% at protein level) to MHC class I molecules. Antigen modulation and sequential immunoprecipitation experiments revealed that LA45 and HLA class I proteins do not crossreact with the corresponding antibodies. Furthermore, LA45 is not associated with beta 2-m. On the other hand, we could show that the separation of HLA-A,B,C and beta 2m molecules, induced by SDS-denaturation, leads to a conformational change in the heavy chain in such a way that it becomes reactive with LA45. The 90/45 kD LA45 proteins thus appear to be non-beta 2m- associated MHC class I alpha chains that are selectively expressed by activated but not by resting human T lymphocytes. |
format | Text |
id | pubmed-2187879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1990 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21878792008-04-17 Activated human T lymphocytes express MHC class I heavy chains not associated with beta 2-microglobulin J Exp Med Articles We present here the molecular characterization of a new activation- induced surface structure on human T lymphocytes, termed LA45, with high homology (93% at protein level) to MHC class I molecules. Antigen modulation and sequential immunoprecipitation experiments revealed that LA45 and HLA class I proteins do not crossreact with the corresponding antibodies. Furthermore, LA45 is not associated with beta 2-m. On the other hand, we could show that the separation of HLA-A,B,C and beta 2m molecules, induced by SDS-denaturation, leads to a conformational change in the heavy chain in such a way that it becomes reactive with LA45. The 90/45 kD LA45 proteins thus appear to be non-beta 2m- associated MHC class I alpha chains that are selectively expressed by activated but not by resting human T lymphocytes. The Rockefeller University Press 1990-05-01 /pmc/articles/PMC2187879/ /pubmed/2139695 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 Activated human T lymphocytes express MHC class I heavy chains not associated with beta 2-microglobulin |
title | Activated human T lymphocytes express MHC class I heavy chains not associated with beta 2-microglobulin |
title_full | Activated human T lymphocytes express MHC class I heavy chains not associated with beta 2-microglobulin |
title_fullStr | Activated human T lymphocytes express MHC class I heavy chains not associated with beta 2-microglobulin |
title_full_unstemmed | Activated human T lymphocytes express MHC class I heavy chains not associated with beta 2-microglobulin |
title_short | Activated human T lymphocytes express MHC class I heavy chains not associated with beta 2-microglobulin |
title_sort | activated human t lymphocytes express mhc class i heavy chains not associated with beta 2-microglobulin |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187879/ https://www.ncbi.nlm.nih.gov/pubmed/2139695 |