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Regulation of B Lymphocyte Development by the Truncated Immunoglobulin Heavy Chain Protein Dμ

The development of B lymphocytes from progenitor cells is dependent on the expression of a pre–B cell–specific receptor made up by a μ heavy chain associated with the surrogate light chains, immunoglobulin (Ig)α, and Igβ. A variant pre–B cell receptor can be formed in which the μ heavy chain is exch...

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Detalles Bibliográficos
Autores principales: Tornberg, Ulla-Carin, Bergqvist, Ingela, Haury, Matthias, Holmberg, Dan
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212169/
https://www.ncbi.nlm.nih.gov/pubmed/9480980
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author Tornberg, Ulla-Carin
Bergqvist, Ingela
Haury, Matthias
Holmberg, Dan
author_facet Tornberg, Ulla-Carin
Bergqvist, Ingela
Haury, Matthias
Holmberg, Dan
author_sort Tornberg, Ulla-Carin
collection PubMed
description The development of B lymphocytes from progenitor cells is dependent on the expression of a pre–B cell–specific receptor made up by a μ heavy chain associated with the surrogate light chains, immunoglobulin (Ig)α, and Igβ. A variant pre–B cell receptor can be formed in which the μ heavy chain is exchanged for a truncated μ chain denoted Dμ. To investigate the role of this receptor in the development of B cells, we have generated transgenic mice that express the Dμ protein in cells of the B lineage. Analysis of these mice reveal that Dμ expression leads to a partial block in B cell development at the early pre–B cell stage, probably by inhibiting V(H) to D(H)J(H) rearrangement. Furthermore, we provide evidence that Dμ induces V(L) to J(L) rearrangements.
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spelling pubmed-22121692008-04-16 Regulation of B Lymphocyte Development by the Truncated Immunoglobulin Heavy Chain Protein Dμ Tornberg, Ulla-Carin Bergqvist, Ingela Haury, Matthias Holmberg, Dan J Exp Med Article The development of B lymphocytes from progenitor cells is dependent on the expression of a pre–B cell–specific receptor made up by a μ heavy chain associated with the surrogate light chains, immunoglobulin (Ig)α, and Igβ. A variant pre–B cell receptor can be formed in which the μ heavy chain is exchanged for a truncated μ chain denoted Dμ. To investigate the role of this receptor in the development of B cells, we have generated transgenic mice that express the Dμ protein in cells of the B lineage. Analysis of these mice reveal that Dμ expression leads to a partial block in B cell development at the early pre–B cell stage, probably by inhibiting V(H) to D(H)J(H) rearrangement. Furthermore, we provide evidence that Dμ induces V(L) to J(L) rearrangements. The Rockefeller University Press 1998-03-02 /pmc/articles/PMC2212169/ /pubmed/9480980 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 Article
Tornberg, Ulla-Carin
Bergqvist, Ingela
Haury, Matthias
Holmberg, Dan
Regulation of B Lymphocyte Development by the Truncated Immunoglobulin Heavy Chain Protein Dμ
title Regulation of B Lymphocyte Development by the Truncated Immunoglobulin Heavy Chain Protein Dμ
title_full Regulation of B Lymphocyte Development by the Truncated Immunoglobulin Heavy Chain Protein Dμ
title_fullStr Regulation of B Lymphocyte Development by the Truncated Immunoglobulin Heavy Chain Protein Dμ
title_full_unstemmed Regulation of B Lymphocyte Development by the Truncated Immunoglobulin Heavy Chain Protein Dμ
title_short Regulation of B Lymphocyte Development by the Truncated Immunoglobulin Heavy Chain Protein Dμ
title_sort regulation of b lymphocyte development by the truncated immunoglobulin heavy chain protein dμ
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212169/
https://www.ncbi.nlm.nih.gov/pubmed/9480980
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