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Interleukin 4 induces changes in the chromatin structure of the gamma 1 switch region in resting B cells before switch recombination

Interleukin 4 (IL-4) can induce the expression of IgG1 in sIgG- murine B cells stimulated with mitogens or through a cognate interaction with T helper (Th) cells. We have investigated the molecular basis for the IL-4-induced switch to IgG1 in lipopolysaccharide (LPS)-stimulated murine B cells and ha...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188184/
https://www.ncbi.nlm.nih.gov/pubmed/2358783
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collection PubMed
description Interleukin 4 (IL-4) can induce the expression of IgG1 in sIgG- murine B cells stimulated with mitogens or through a cognate interaction with T helper (Th) cells. We have investigated the molecular basis for the IL-4-induced switch to IgG1 in lipopolysaccharide (LPS)-stimulated murine B cells and have previously shown that IL-4 induces transcription of the gamma 1 switch region before switch recombination. We now demonstrate that IL-4 induces a DNase I hypersensitive site at the 5' end of the gamma 1 switch region in resting B cells. LPS is not required, but it enhances induction. Hence, the interaction of IL-4 with its receptor results in increased accessibility of the gamma 1 switch region. The more open chromatin structure and increased transcriptional activity may be important in the selection of this region for switch recombination.
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spelling pubmed-21881842008-04-17 Interleukin 4 induces changes in the chromatin structure of the gamma 1 switch region in resting B cells before switch recombination J Exp Med Articles Interleukin 4 (IL-4) can induce the expression of IgG1 in sIgG- murine B cells stimulated with mitogens or through a cognate interaction with T helper (Th) cells. We have investigated the molecular basis for the IL-4-induced switch to IgG1 in lipopolysaccharide (LPS)-stimulated murine B cells and have previously shown that IL-4 induces transcription of the gamma 1 switch region before switch recombination. We now demonstrate that IL-4 induces a DNase I hypersensitive site at the 5' end of the gamma 1 switch region in resting B cells. LPS is not required, but it enhances induction. Hence, the interaction of IL-4 with its receptor results in increased accessibility of the gamma 1 switch region. The more open chromatin structure and increased transcriptional activity may be important in the selection of this region for switch recombination. The Rockefeller University Press 1990-07-01 /pmc/articles/PMC2188184/ /pubmed/2358783 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
Interleukin 4 induces changes in the chromatin structure of the gamma 1 switch region in resting B cells before switch recombination
title Interleukin 4 induces changes in the chromatin structure of the gamma 1 switch region in resting B cells before switch recombination
title_full Interleukin 4 induces changes in the chromatin structure of the gamma 1 switch region in resting B cells before switch recombination
title_fullStr Interleukin 4 induces changes in the chromatin structure of the gamma 1 switch region in resting B cells before switch recombination
title_full_unstemmed Interleukin 4 induces changes in the chromatin structure of the gamma 1 switch region in resting B cells before switch recombination
title_short Interleukin 4 induces changes in the chromatin structure of the gamma 1 switch region in resting B cells before switch recombination
title_sort interleukin 4 induces changes in the chromatin structure of the gamma 1 switch region in resting b cells before switch recombination
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188184/
https://www.ncbi.nlm.nih.gov/pubmed/2358783