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Counterselection against Dμ Is Mediated through Immunoglobulin (Ig)α-Igβ

The pre-B cell receptor is a key checkpoint regulator in developing B cells. Early events that are controlled by the pre-B cell receptor include positive selection for cells express membrane immunoglobulin heavy chains and negative selection against cells expressing truncated immunoglobulins that la...

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Detalles Bibliográficos
Autores principales: Gong, Shiaoching, Sanchez, Mercedes, Nussenzweig, Michel C.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196397/
https://www.ncbi.nlm.nih.gov/pubmed/8976164
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author Gong, Shiaoching
Sanchez, Mercedes
Nussenzweig, Michel C.
author_facet Gong, Shiaoching
Sanchez, Mercedes
Nussenzweig, Michel C.
author_sort Gong, Shiaoching
collection PubMed
description The pre-B cell receptor is a key checkpoint regulator in developing B cells. Early events that are controlled by the pre-B cell receptor include positive selection for cells express membrane immunoglobulin heavy chains and negative selection against cells expressing truncated immunoglobulins that lack a complete variable region (Dμ). Positive selection is known to be mediated by membrane immunoglobulin heavy chains through Igα-Igβ, whereas the mechanism for counterselection against Dμ has not been determined. We have examined the role of the Igα-Igβ signal transducers in counterselection against Dμ using mice that lack Igβ. We found that Dμ expression is not selected against in developing B cells in Igβ mutant mice. Thus, the molecular mechanism for counterselection against Dμ in pre-B cells resembles positive selection in that it requires interaction between mDμ and Igα-Igβ.
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spelling pubmed-21963972008-04-16 Counterselection against Dμ Is Mediated through Immunoglobulin (Ig)α-Igβ Gong, Shiaoching Sanchez, Mercedes Nussenzweig, Michel C. J Exp Med Article The pre-B cell receptor is a key checkpoint regulator in developing B cells. Early events that are controlled by the pre-B cell receptor include positive selection for cells express membrane immunoglobulin heavy chains and negative selection against cells expressing truncated immunoglobulins that lack a complete variable region (Dμ). Positive selection is known to be mediated by membrane immunoglobulin heavy chains through Igα-Igβ, whereas the mechanism for counterselection against Dμ has not been determined. We have examined the role of the Igα-Igβ signal transducers in counterselection against Dμ using mice that lack Igβ. We found that Dμ expression is not selected against in developing B cells in Igβ mutant mice. Thus, the molecular mechanism for counterselection against Dμ in pre-B cells resembles positive selection in that it requires interaction between mDμ and Igα-Igβ. The Rockefeller University Press 1996-12-01 /pmc/articles/PMC2196397/ /pubmed/8976164 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
Gong, Shiaoching
Sanchez, Mercedes
Nussenzweig, Michel C.
Counterselection against Dμ Is Mediated through Immunoglobulin (Ig)α-Igβ
title Counterselection against Dμ Is Mediated through Immunoglobulin (Ig)α-Igβ
title_full Counterselection against Dμ Is Mediated through Immunoglobulin (Ig)α-Igβ
title_fullStr Counterselection against Dμ Is Mediated through Immunoglobulin (Ig)α-Igβ
title_full_unstemmed Counterselection against Dμ Is Mediated through Immunoglobulin (Ig)α-Igβ
title_short Counterselection against Dμ Is Mediated through Immunoglobulin (Ig)α-Igβ
title_sort counterselection against dμ is mediated through immunoglobulin (ig)α-igβ
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196397/
https://www.ncbi.nlm.nih.gov/pubmed/8976164
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