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FK506 inhibits antigen receptor-mediated induction of c-rel in B and T lymphoid cells

Stimulation of B and T cells via the antigen receptor, by phorbol ester or by phorbol ester and ionomycin, leads to nuclear translocation of the inducible transcription factor NF-kappa B, comprising the p50 and p65 rel-related polypeptides. In this report we show that c-rel is a component of the ant...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191924/
https://www.ncbi.nlm.nih.gov/pubmed/7532676
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description Stimulation of B and T cells via the antigen receptor, by phorbol ester or by phorbol ester and ionomycin, leads to nuclear translocation of the inducible transcription factor NF-kappa B, comprising the p50 and p65 rel-related polypeptides. In this report we show that c-rel is a component of the antigen receptor-induced kappa B binding proteins in both B and T cells. Whereas NF-kappa B can be induced by phorbol ester alone, optimal induction of c-rel requires stimulation by both phorbol ester and ionomycin, the dual signal that is necessary for proliferation of untransformed lymphocytes. Furthermore, c-rel induction is blocked by the immunosuppressive drug FK506 that is known to inhibit B and T cell activation. c-rel-dependent transactivation of the interleukin-2 receptor alpha chain (IL-2R alpha) promoter is augmented by coexpression of calcineurin, suggesting the involvement of a calcineurin-dependent intracellular pathway. Our results identify c- rel as a target of immunosuppressive agents and illustrate the similarity of activation pathways in both B and T cells.
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spelling pubmed-21919242008-04-16 FK506 inhibits antigen receptor-mediated induction of c-rel in B and T lymphoid cells J Exp Med Articles Stimulation of B and T cells via the antigen receptor, by phorbol ester or by phorbol ester and ionomycin, leads to nuclear translocation of the inducible transcription factor NF-kappa B, comprising the p50 and p65 rel-related polypeptides. In this report we show that c-rel is a component of the antigen receptor-induced kappa B binding proteins in both B and T cells. Whereas NF-kappa B can be induced by phorbol ester alone, optimal induction of c-rel requires stimulation by both phorbol ester and ionomycin, the dual signal that is necessary for proliferation of untransformed lymphocytes. Furthermore, c-rel induction is blocked by the immunosuppressive drug FK506 that is known to inhibit B and T cell activation. c-rel-dependent transactivation of the interleukin-2 receptor alpha chain (IL-2R alpha) promoter is augmented by coexpression of calcineurin, suggesting the involvement of a calcineurin-dependent intracellular pathway. Our results identify c- rel as a target of immunosuppressive agents and illustrate the similarity of activation pathways in both B and T cells. The Rockefeller University Press 1995-03-01 /pmc/articles/PMC2191924/ /pubmed/7532676 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
FK506 inhibits antigen receptor-mediated induction of c-rel in B and T lymphoid cells
title FK506 inhibits antigen receptor-mediated induction of c-rel in B and T lymphoid cells
title_full FK506 inhibits antigen receptor-mediated induction of c-rel in B and T lymphoid cells
title_fullStr FK506 inhibits antigen receptor-mediated induction of c-rel in B and T lymphoid cells
title_full_unstemmed FK506 inhibits antigen receptor-mediated induction of c-rel in B and T lymphoid cells
title_short FK506 inhibits antigen receptor-mediated induction of c-rel in B and T lymphoid cells
title_sort fk506 inhibits antigen receptor-mediated induction of c-rel in b and t lymphoid cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191924/
https://www.ncbi.nlm.nih.gov/pubmed/7532676