Cargando…

Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations

The nonimmune adult spleen contains at least two B-cell subpopulations. The majority of primary B cells express cell surface Ia determinants and have the capacity to give rise to IgG antibody-producing clones after T-cell dependent antigenic stimulation. There is also a small subpopulation of primar...

Descripción completa

Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1976
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190390/
https://www.ncbi.nlm.nih.gov/pubmed/1085328
_version_ 1782146792892137472
collection PubMed
description The nonimmune adult spleen contains at least two B-cell subpopulations. The majority of primary B cells express cell surface Ia determinants and have the capacity to give rise to IgG antibody-producing clones after T-cell dependent antigenic stimulation. There is also a small subpopulation of primary B cells which are, by definition, Ia negative, since their activity is not eliminated by negative selection with anti- Ia serum and complement. The Ia-negative B cells give rise to clones that produce only IgM antibody. These B-cell subsets may form a continuum in B-cell maturation, or they may exist as discrete B-cell lineages. Since the cellular expression of Ia antigens appears to correlate with the ability of the B cell to generate IgG-producing clones, it is speculated that Ia molecules may have a role in the IgM to IgG B-cell switch mechanism.
format Text
id pubmed-2190390
institution National Center for Biotechnology Information
language English
publishDate 1976
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21903902008-04-17 Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations J Exp Med Articles The nonimmune adult spleen contains at least two B-cell subpopulations. The majority of primary B cells express cell surface Ia determinants and have the capacity to give rise to IgG antibody-producing clones after T-cell dependent antigenic stimulation. There is also a small subpopulation of primary B cells which are, by definition, Ia negative, since their activity is not eliminated by negative selection with anti- Ia serum and complement. The Ia-negative B cells give rise to clones that produce only IgM antibody. These B-cell subsets may form a continuum in B-cell maturation, or they may exist as discrete B-cell lineages. Since the cellular expression of Ia antigens appears to correlate with the ability of the B cell to generate IgG-producing clones, it is speculated that Ia molecules may have a role in the IgM to IgG B-cell switch mechanism. The Rockefeller University Press 1976-08-01 /pmc/articles/PMC2190390/ /pubmed/1085328 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
Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations
title Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations
title_full Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations
title_fullStr Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations
title_full_unstemmed Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations
title_short Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations
title_sort expression of ia antigens on hapten-specific b cells. i. delineation of b-cell subpopulations
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190390/
https://www.ncbi.nlm.nih.gov/pubmed/1085328