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spelling todo:paper_00137227_v147_n11_p5452_Presman2023-10-03T14:11:18Z Melatonin inhibits glucocorticoid receptor nuclear translocation in mouse thymocytes Presman, D.M. Hoijman, E. Ceballos, N.R. Galigniana, M.D. Pecci, A. cell nucleus receptor cytochrome c dexamethasone glucocorticoid receptor heat shock protein 90 indole derivative melatonin messenger RNA methoxyindole orphan nuclear receptor ROR alpha protein Bax retinoid unclassified drug animal cell animal experiment article breast epithelium controlled study drug inhibition drug mechanism gene expression gene translocation immunoprecipitation ligand binding male mouse nonhuman priority journal thymocyte transcription initiation Active Transport, Cell Nucleus Animals Apoptosis Cell Nucleus Dexamethasone Male Melatonin Mice Protein Transport Receptors, Glucocorticoid T-Lymphocytes Thymus Gland The antiapoptotic effect of melatonin (MEL) has been described in several systems. In particular, MEL inhibits glucocorticoid-mediated apoptosis. Our group previously demonstrated that in the thymus, MEL inhibits the release of Cytochrome C from mitochondria and the dexamethasone-dependent increase of bax mRNA levels. In this study we analyzed the ability of MEL to regulate the activation of the glucocorticoid receptor (GR) in mouse thymocytes. We found that even though the methoxyindole does not affect the ligand binding capacity of the receptor, it impairs the steroid-dependent nuclear translocation of the GR and also prevents transformation by blocking the dissociation of the 90-kDa heat shock protein. Coincubation of the methoxyindole with dexamethasone did not affect the expression of a reporter gene in GR-transfected Cos-7 cells or HC11 and L929 mouse cell lines that express Mel-1a and retinoid-related orphan receptor-α (RORα) receptors. Therefore, the antagonistic effect of MEL seems to be specific for thymocytes, in a Mel 1a- and RORα-independent manner. In summary, the present results suggest a novel mechanism for the antagonistic action of MEL on GR-mediated effects, which involves the inhibition of 90-kDa heat shock protein dissociation and the cytoplasmic retention of the GR. Copyright © 2006 by The Endocrine Society. Fil:Presman, D.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Hoijman, E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Ceballos, N.R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Pecci, 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_00137227_v147_n11_p5452_Presman
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic cell nucleus receptor
cytochrome c
dexamethasone
glucocorticoid receptor
heat shock protein 90
indole derivative
melatonin
messenger RNA
methoxyindole
orphan nuclear receptor ROR alpha
protein Bax
retinoid
unclassified drug
animal cell
animal experiment
article
breast epithelium
controlled study
drug inhibition
drug mechanism
gene expression
gene translocation
immunoprecipitation
ligand binding
male
mouse
nonhuman
priority journal
thymocyte
transcription initiation
Active Transport, Cell Nucleus
Animals
Apoptosis
Cell Nucleus
Dexamethasone
Male
Melatonin
Mice
Protein Transport
Receptors, Glucocorticoid
T-Lymphocytes
Thymus Gland
spellingShingle cell nucleus receptor
cytochrome c
dexamethasone
glucocorticoid receptor
heat shock protein 90
indole derivative
melatonin
messenger RNA
methoxyindole
orphan nuclear receptor ROR alpha
protein Bax
retinoid
unclassified drug
animal cell
animal experiment
article
breast epithelium
controlled study
drug inhibition
drug mechanism
gene expression
gene translocation
immunoprecipitation
ligand binding
male
mouse
nonhuman
priority journal
thymocyte
transcription initiation
Active Transport, Cell Nucleus
Animals
Apoptosis
Cell Nucleus
Dexamethasone
Male
Melatonin
Mice
Protein Transport
Receptors, Glucocorticoid
T-Lymphocytes
Thymus Gland
Presman, D.M.
Hoijman, E.
Ceballos, N.R.
Galigniana, M.D.
Pecci, A.
Melatonin inhibits glucocorticoid receptor nuclear translocation in mouse thymocytes
topic_facet cell nucleus receptor
cytochrome c
dexamethasone
glucocorticoid receptor
heat shock protein 90
indole derivative
melatonin
messenger RNA
methoxyindole
orphan nuclear receptor ROR alpha
protein Bax
retinoid
unclassified drug
animal cell
animal experiment
article
breast epithelium
controlled study
drug inhibition
drug mechanism
gene expression
gene translocation
immunoprecipitation
ligand binding
male
mouse
nonhuman
priority journal
thymocyte
transcription initiation
Active Transport, Cell Nucleus
Animals
Apoptosis
Cell Nucleus
Dexamethasone
Male
Melatonin
Mice
Protein Transport
Receptors, Glucocorticoid
T-Lymphocytes
Thymus Gland
description The antiapoptotic effect of melatonin (MEL) has been described in several systems. In particular, MEL inhibits glucocorticoid-mediated apoptosis. Our group previously demonstrated that in the thymus, MEL inhibits the release of Cytochrome C from mitochondria and the dexamethasone-dependent increase of bax mRNA levels. In this study we analyzed the ability of MEL to regulate the activation of the glucocorticoid receptor (GR) in mouse thymocytes. We found that even though the methoxyindole does not affect the ligand binding capacity of the receptor, it impairs the steroid-dependent nuclear translocation of the GR and also prevents transformation by blocking the dissociation of the 90-kDa heat shock protein. Coincubation of the methoxyindole with dexamethasone did not affect the expression of a reporter gene in GR-transfected Cos-7 cells or HC11 and L929 mouse cell lines that express Mel-1a and retinoid-related orphan receptor-α (RORα) receptors. Therefore, the antagonistic effect of MEL seems to be specific for thymocytes, in a Mel 1a- and RORα-independent manner. In summary, the present results suggest a novel mechanism for the antagonistic action of MEL on GR-mediated effects, which involves the inhibition of 90-kDa heat shock protein dissociation and the cytoplasmic retention of the GR. Copyright © 2006 by The Endocrine Society.
format JOUR
author Presman, D.M.
Hoijman, E.
Ceballos, N.R.
Galigniana, M.D.
Pecci, A.
author_facet Presman, D.M.
Hoijman, E.
Ceballos, N.R.
Galigniana, M.D.
Pecci, A.
author_sort Presman, D.M.
title Melatonin inhibits glucocorticoid receptor nuclear translocation in mouse thymocytes
title_short Melatonin inhibits glucocorticoid receptor nuclear translocation in mouse thymocytes
title_full Melatonin inhibits glucocorticoid receptor nuclear translocation in mouse thymocytes
title_fullStr Melatonin inhibits glucocorticoid receptor nuclear translocation in mouse thymocytes
title_full_unstemmed Melatonin inhibits glucocorticoid receptor nuclear translocation in mouse thymocytes
title_sort melatonin inhibits glucocorticoid receptor nuclear translocation in mouse thymocytes
url http://hdl.handle.net/20.500.12110/paper_00137227_v147_n11_p5452_Presman
work_keys_str_mv AT presmandm melatonininhibitsglucocorticoidreceptornucleartranslocationinmousethymocytes
AT hoijmane melatonininhibitsglucocorticoidreceptornucleartranslocationinmousethymocytes
AT ceballosnr melatonininhibitsglucocorticoidreceptornucleartranslocationinmousethymocytes
AT galignianamd melatonininhibitsglucocorticoidreceptornucleartranslocationinmousethymocytes
AT peccia melatonininhibitsglucocorticoidreceptornucleartranslocationinmousethymocytes
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