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The role of gene products of the I-J subregion in mixed lymphocyte reactions

We have examined the MLR reaction in two sets of recombinants that differ in the I-J subregion. In both cases, significant stimulation was mediated by antigens controlled by genes in the I-J subregion. This stimulation was inhibitable by the addition of the culture of antisera directed against the I...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1977
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2181912/
https://www.ncbi.nlm.nih.gov/pubmed/144771
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description We have examined the MLR reaction in two sets of recombinants that differ in the I-J subregion. In both cases, significant stimulation was mediated by antigens controlled by genes in the I-J subregion. This stimulation was inhibitable by the addition of the culture of antisera directed against the I-J gene products on the stimulator cell. The specificity of this inhibition was shown by specific blocking of the relevant gene product on F1 hybrid stimulator cells. MLR stimulation was also eliminated by pretreatment of the stimulator population with anti-I-J sera plus complement. Pretreatment of F1 hybrid stimulator T cells with anti-I-J sera directed against either parental I-J product in the presence of complement, completely eliminated stimulation, indicating that there is no allelic exclusion of the relevant I-J products. Pretreatment with an anti-I-E/I-C serum and complement also eliminated stimulation, suggesting that the stimulating T cells express both I-J and I-E/I-C subregion products. This assay offers a potentially more direct and practical method for serological detection of the I-J products.
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spelling pubmed-21819122008-04-17 The role of gene products of the I-J subregion in mixed lymphocyte reactions J Exp Med Articles We have examined the MLR reaction in two sets of recombinants that differ in the I-J subregion. In both cases, significant stimulation was mediated by antigens controlled by genes in the I-J subregion. This stimulation was inhibitable by the addition of the culture of antisera directed against the I-J gene products on the stimulator cell. The specificity of this inhibition was shown by specific blocking of the relevant gene product on F1 hybrid stimulator cells. MLR stimulation was also eliminated by pretreatment of the stimulator population with anti-I-J sera plus complement. Pretreatment of F1 hybrid stimulator T cells with anti-I-J sera directed against either parental I-J product in the presence of complement, completely eliminated stimulation, indicating that there is no allelic exclusion of the relevant I-J products. Pretreatment with an anti-I-E/I-C serum and complement also eliminated stimulation, suggesting that the stimulating T cells express both I-J and I-E/I-C subregion products. This assay offers a potentially more direct and practical method for serological detection of the I-J products. The Rockefeller University Press 1977-12-01 /pmc/articles/PMC2181912/ /pubmed/144771 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
The role of gene products of the I-J subregion in mixed lymphocyte reactions
title The role of gene products of the I-J subregion in mixed lymphocyte reactions
title_full The role of gene products of the I-J subregion in mixed lymphocyte reactions
title_fullStr The role of gene products of the I-J subregion in mixed lymphocyte reactions
title_full_unstemmed The role of gene products of the I-J subregion in mixed lymphocyte reactions
title_short The role of gene products of the I-J subregion in mixed lymphocyte reactions
title_sort role of gene products of the i-j subregion in mixed lymphocyte reactions
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2181912/
https://www.ncbi.nlm.nih.gov/pubmed/144771