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Mitogen-reactive B cell subpopulations selectively express different sets of V regions

The experiments presented here were designed to investigate whether the idiotypic repertoire is equally distributed among B cells subpopulations as defined by mitogen reactivity. To this end we used lipopolysaccharides (LPS) and Nocardia delipidated cell mitogens (NDCM), which are two mitogens that...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1982
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186741/
https://www.ncbi.nlm.nih.gov/pubmed/6979604
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collection PubMed
description The experiments presented here were designed to investigate whether the idiotypic repertoire is equally distributed among B cells subpopulations as defined by mitogen reactivity. To this end we used lipopolysaccharides (LPS) and Nocardia delipidated cell mitogens (NDCM), which are two mitogens that have been described to act on different B cell subsets. The repertoire can be defined in quantitative terms as the frequency of B cells that are precursors for clones secreting immunoglobulin with a given specificity or with a determinate idiotype. We determined, therefore, the absolute frequency of LPS- and NDCM-sensitive B lymphocytes secreting immunoglobulin molecules that bear three idiotopes originally found on a monoclonal anti-beta galactosidase antibody. Because the frequencies of B cells carrying one of these idiotypes are dramatically different in the LPS- and NDCM- sensitive B cells subsets, we conclude that the idiotypic repertoire is not randomly distributed among mitogen-reactive B cell subpopulations.
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spelling pubmed-21867412008-04-17 Mitogen-reactive B cell subpopulations selectively express different sets of V regions J Exp Med Articles The experiments presented here were designed to investigate whether the idiotypic repertoire is equally distributed among B cells subpopulations as defined by mitogen reactivity. To this end we used lipopolysaccharides (LPS) and Nocardia delipidated cell mitogens (NDCM), which are two mitogens that have been described to act on different B cell subsets. The repertoire can be defined in quantitative terms as the frequency of B cells that are precursors for clones secreting immunoglobulin with a given specificity or with a determinate idiotype. We determined, therefore, the absolute frequency of LPS- and NDCM-sensitive B lymphocytes secreting immunoglobulin molecules that bear three idiotopes originally found on a monoclonal anti-beta galactosidase antibody. Because the frequencies of B cells carrying one of these idiotypes are dramatically different in the LPS- and NDCM- sensitive B cells subsets, we conclude that the idiotypic repertoire is not randomly distributed among mitogen-reactive B cell subpopulations. The Rockefeller University Press 1982-07-01 /pmc/articles/PMC2186741/ /pubmed/6979604 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
Mitogen-reactive B cell subpopulations selectively express different sets of V regions
title Mitogen-reactive B cell subpopulations selectively express different sets of V regions
title_full Mitogen-reactive B cell subpopulations selectively express different sets of V regions
title_fullStr Mitogen-reactive B cell subpopulations selectively express different sets of V regions
title_full_unstemmed Mitogen-reactive B cell subpopulations selectively express different sets of V regions
title_short Mitogen-reactive B cell subpopulations selectively express different sets of V regions
title_sort mitogen-reactive b cell subpopulations selectively express different sets of v regions
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186741/
https://www.ncbi.nlm.nih.gov/pubmed/6979604