CRE-Mediated transcriptional activation is involved in cAMP protection of T-cell receptor-induced apoptosis but not in cAMP potentiation of glucocorticoid-mediated programmed cell death

Apoptosis of thymic cells induced by glucocorticoids (GC) and T-cell receptor (TCR) engagement are mutually antagonistic. We demonstrate that cAMP enhances GC and antagonizes TCR (anti-CD3) apoptosis on the same cell (DO-11.10 and 2B4.11 T-cell hybridomas). We analyzed the activity of several transc...

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Autores principales: Igaz, L.M., Refojo, D., Costas, M.A., Holsboer, F., Arzt, E.
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spelling todo:paper_01674889_v1542_n1-3_p139_Igaz2023-10-03T15:04:48Z CRE-Mediated transcriptional activation is involved in cAMP protection of T-cell receptor-induced apoptosis but not in cAMP potentiation of glucocorticoid-mediated programmed cell death Igaz, L.M. Refojo, D. Costas, M.A. Holsboer, F. Arzt, E. Apoptosis CAMP responsive element binding protein Cyclic AMP Glucocorticoids T cell receptor bucladesine CD3 antigen cyclic AMP cyclic AMP responsive element binding protein dexamethasone DNA glucocorticoid immunoglobulin enhancer binding protein monoclonal antibody CD3 oligomer T lymphocyte receptor animal cell apoptosis article controlled study cyclic AMP responsive element enzyme activity enzyme inhibition genetic transfection hybridoma cell culture mouse nonhuman priority journal regulatory mechanism T lymphocyte transcription initiation Animals Apoptosis Cell Line Cyclic AMP Cyclic AMP Response Element-Binding Protein Flow Cytometry Glucocorticoids Hybridomas Mice Receptors, Antigen, T-Cell Response Elements T-Lymphocytes Transcription, Genetic Transfection Apoptosis of thymic cells induced by glucocorticoids (GC) and T-cell receptor (TCR) engagement are mutually antagonistic. We demonstrate that cAMP enhances GC and antagonizes TCR (anti-CD3) apoptosis on the same cell (DO-11.10 and 2B4.11 T-cell hybridomas). We analyzed the activity of several transcription factors in this cAMP dual, stimulus-dependent, regulatory action. Anti-CD3 increases kB-activity which is inhibited by CPTcAMP or dexamethasone (DEX), supporting the proapoptotic role of NFkB on TCR-induced apoptosis. Anti-CD3 not only increases kB- but diminishes GC response element (GRE)-activity induced by DEX, suggesting that TCR-mediated blockade of GC-induced apoptosis involves not only the proposed antiapoptotic action of NF-kB on GC, but also the inhibition of GRE-regulated proapoptotic genes. To test the involvement of CRE-driven transcription in the cAMP dual apoptotic regulation, cells were transfected with a CRE decoy DNA oligomer. Blockade of CRE transactivation with decoy targeting of CRE completely blocked the protection of TCR-induced apoptosis by cAMP, while it did not modify the enhancement by cAMP on GC-induced apoptosis. We show that CRE-binding factors have a definite role in T-cell apoptosis: they are involved in cAMP protection of TCR- but not in cAMP potentiation of GC-induced apoptosis. © 2002 Elsevier Science B.V. All rights reserved. Fil:Refojo, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Costas, M.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01674889_v1542_n1-3_p139_Igaz
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Apoptosis
CAMP responsive element binding protein
Cyclic AMP
Glucocorticoids
T cell receptor
bucladesine
CD3 antigen
cyclic AMP
cyclic AMP responsive element binding protein
dexamethasone
DNA
glucocorticoid
immunoglobulin enhancer binding protein
monoclonal antibody CD3
oligomer
T lymphocyte receptor
animal cell
apoptosis
article
controlled study
cyclic AMP responsive element
enzyme activity
enzyme inhibition
genetic transfection
hybridoma cell culture
mouse
nonhuman
priority journal
regulatory mechanism
T lymphocyte
transcription initiation
Animals
Apoptosis
Cell Line
Cyclic AMP
Cyclic AMP Response Element-Binding Protein
Flow Cytometry
Glucocorticoids
Hybridomas
Mice
Receptors, Antigen, T-Cell
Response Elements
T-Lymphocytes
Transcription, Genetic
Transfection
spellingShingle Apoptosis
CAMP responsive element binding protein
Cyclic AMP
Glucocorticoids
T cell receptor
bucladesine
CD3 antigen
cyclic AMP
cyclic AMP responsive element binding protein
dexamethasone
DNA
glucocorticoid
immunoglobulin enhancer binding protein
monoclonal antibody CD3
oligomer
T lymphocyte receptor
animal cell
apoptosis
article
controlled study
cyclic AMP responsive element
enzyme activity
enzyme inhibition
genetic transfection
hybridoma cell culture
mouse
nonhuman
priority journal
regulatory mechanism
T lymphocyte
transcription initiation
Animals
Apoptosis
Cell Line
Cyclic AMP
Cyclic AMP Response Element-Binding Protein
Flow Cytometry
Glucocorticoids
Hybridomas
Mice
Receptors, Antigen, T-Cell
Response Elements
T-Lymphocytes
Transcription, Genetic
Transfection
Igaz, L.M.
Refojo, D.
Costas, M.A.
Holsboer, F.
Arzt, E.
CRE-Mediated transcriptional activation is involved in cAMP protection of T-cell receptor-induced apoptosis but not in cAMP potentiation of glucocorticoid-mediated programmed cell death
topic_facet Apoptosis
CAMP responsive element binding protein
Cyclic AMP
Glucocorticoids
T cell receptor
bucladesine
CD3 antigen
cyclic AMP
cyclic AMP responsive element binding protein
dexamethasone
DNA
glucocorticoid
immunoglobulin enhancer binding protein
monoclonal antibody CD3
oligomer
T lymphocyte receptor
animal cell
apoptosis
article
controlled study
cyclic AMP responsive element
enzyme activity
enzyme inhibition
genetic transfection
hybridoma cell culture
mouse
nonhuman
priority journal
regulatory mechanism
T lymphocyte
transcription initiation
Animals
Apoptosis
Cell Line
Cyclic AMP
Cyclic AMP Response Element-Binding Protein
Flow Cytometry
Glucocorticoids
Hybridomas
Mice
Receptors, Antigen, T-Cell
Response Elements
T-Lymphocytes
Transcription, Genetic
Transfection
description Apoptosis of thymic cells induced by glucocorticoids (GC) and T-cell receptor (TCR) engagement are mutually antagonistic. We demonstrate that cAMP enhances GC and antagonizes TCR (anti-CD3) apoptosis on the same cell (DO-11.10 and 2B4.11 T-cell hybridomas). We analyzed the activity of several transcription factors in this cAMP dual, stimulus-dependent, regulatory action. Anti-CD3 increases kB-activity which is inhibited by CPTcAMP or dexamethasone (DEX), supporting the proapoptotic role of NFkB on TCR-induced apoptosis. Anti-CD3 not only increases kB- but diminishes GC response element (GRE)-activity induced by DEX, suggesting that TCR-mediated blockade of GC-induced apoptosis involves not only the proposed antiapoptotic action of NF-kB on GC, but also the inhibition of GRE-regulated proapoptotic genes. To test the involvement of CRE-driven transcription in the cAMP dual apoptotic regulation, cells were transfected with a CRE decoy DNA oligomer. Blockade of CRE transactivation with decoy targeting of CRE completely blocked the protection of TCR-induced apoptosis by cAMP, while it did not modify the enhancement by cAMP on GC-induced apoptosis. We show that CRE-binding factors have a definite role in T-cell apoptosis: they are involved in cAMP protection of TCR- but not in cAMP potentiation of GC-induced apoptosis. © 2002 Elsevier Science B.V. All rights reserved.
format JOUR
author Igaz, L.M.
Refojo, D.
Costas, M.A.
Holsboer, F.
Arzt, E.
author_facet Igaz, L.M.
Refojo, D.
Costas, M.A.
Holsboer, F.
Arzt, E.
author_sort Igaz, L.M.
title CRE-Mediated transcriptional activation is involved in cAMP protection of T-cell receptor-induced apoptosis but not in cAMP potentiation of glucocorticoid-mediated programmed cell death
title_short CRE-Mediated transcriptional activation is involved in cAMP protection of T-cell receptor-induced apoptosis but not in cAMP potentiation of glucocorticoid-mediated programmed cell death
title_full CRE-Mediated transcriptional activation is involved in cAMP protection of T-cell receptor-induced apoptosis but not in cAMP potentiation of glucocorticoid-mediated programmed cell death
title_fullStr CRE-Mediated transcriptional activation is involved in cAMP protection of T-cell receptor-induced apoptosis but not in cAMP potentiation of glucocorticoid-mediated programmed cell death
title_full_unstemmed CRE-Mediated transcriptional activation is involved in cAMP protection of T-cell receptor-induced apoptosis but not in cAMP potentiation of glucocorticoid-mediated programmed cell death
title_sort cre-mediated transcriptional activation is involved in camp protection of t-cell receptor-induced apoptosis but not in camp potentiation of glucocorticoid-mediated programmed cell death
url http://hdl.handle.net/20.500.12110/paper_01674889_v1542_n1-3_p139_Igaz
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AT costasma cremediatedtranscriptionalactivationisinvolvedincampprotectionoftcellreceptorinducedapoptosisbutnotincamppotentiationofglucocorticoidmediatedprogrammedcelldeath
AT holsboerf cremediatedtranscriptionalactivationisinvolvedincampprotectionoftcellreceptorinducedapoptosisbutnotincamppotentiationofglucocorticoidmediatedprogrammedcelldeath
AT arzte cremediatedtranscriptionalactivationisinvolvedincampprotectionoftcellreceptorinducedapoptosisbutnotincamppotentiationofglucocorticoidmediatedprogrammedcelldeath
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