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Sleep Deprivation Alters the Pituitary Stress Transcriptome in Male and Female Mice

Poor sleep hygiene is a growing problem, with detrimental effects on many biological systems. The pituitary gland plays a crucial role in the regulation of sleep and the stress response, and its dysfunction leads to sleep-related disorders. However, the interaction between these critical functions r...

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Autores principales: Oyola, Mario G., Shupe, Elizabeth A., Soltis, Anthony R., Sukumar, Gauthaman, Paez-Pereda, Marcelo, Larco, Darwin O., Wilkerson, Matthew D., Rothwell, Stephen, Dalgard, Clifton L., Wu, T. John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794367/
https://www.ncbi.nlm.nih.gov/pubmed/31649619
http://dx.doi.org/10.3389/fendo.2019.00676
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author Oyola, Mario G.
Shupe, Elizabeth A.
Soltis, Anthony R.
Sukumar, Gauthaman
Paez-Pereda, Marcelo
Larco, Darwin O.
Wilkerson, Matthew D.
Rothwell, Stephen
Dalgard, Clifton L.
Wu, T. John
author_facet Oyola, Mario G.
Shupe, Elizabeth A.
Soltis, Anthony R.
Sukumar, Gauthaman
Paez-Pereda, Marcelo
Larco, Darwin O.
Wilkerson, Matthew D.
Rothwell, Stephen
Dalgard, Clifton L.
Wu, T. John
author_sort Oyola, Mario G.
collection PubMed
description Poor sleep hygiene is a growing problem, with detrimental effects on many biological systems. The pituitary gland plays a crucial role in the regulation of sleep and the stress response, and its dysfunction leads to sleep-related disorders. However, the interaction between these critical functions remains unclear. Thus, we performed a comparative, whole-transcriptome, analysis to identify stress-induced genes and relevant pathways that may be affected by sleep deprivation. One day following 12 h of Paradoxical Sleep Deprivation (PSD), mice were restrained for 20 min. Gene expression changes in the pituitary were assessed via RNA-Seq and Gene Ontology in PSD and/or restrained groups compared to controls. We show that restraint triggers transcriptional responses involved in hormone secretion, the glucocorticoid response, and apoptosis in both sexes, with 285 differentially expressed genes in females and 93 in males. When PSD preceded restraint stress, the numbers of differentially expressed genes increased to 613 in females and 580 in males. The pituitary transcriptome of restraint+PSD animals was enriched for microglia and macrophage proliferation, cellular response to corticosteroids, and apoptosis, among others. Finally, we identify sex-specific differences in restraint-induced genes following PSD. These findings provide genetic targets to consider when studying sleep and the response to stress.
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spelling pubmed-67943672019-10-24 Sleep Deprivation Alters the Pituitary Stress Transcriptome in Male and Female Mice Oyola, Mario G. Shupe, Elizabeth A. Soltis, Anthony R. Sukumar, Gauthaman Paez-Pereda, Marcelo Larco, Darwin O. Wilkerson, Matthew D. Rothwell, Stephen Dalgard, Clifton L. Wu, T. John Front Endocrinol (Lausanne) Endocrinology Poor sleep hygiene is a growing problem, with detrimental effects on many biological systems. The pituitary gland plays a crucial role in the regulation of sleep and the stress response, and its dysfunction leads to sleep-related disorders. However, the interaction between these critical functions remains unclear. Thus, we performed a comparative, whole-transcriptome, analysis to identify stress-induced genes and relevant pathways that may be affected by sleep deprivation. One day following 12 h of Paradoxical Sleep Deprivation (PSD), mice were restrained for 20 min. Gene expression changes in the pituitary were assessed via RNA-Seq and Gene Ontology in PSD and/or restrained groups compared to controls. We show that restraint triggers transcriptional responses involved in hormone secretion, the glucocorticoid response, and apoptosis in both sexes, with 285 differentially expressed genes in females and 93 in males. When PSD preceded restraint stress, the numbers of differentially expressed genes increased to 613 in females and 580 in males. The pituitary transcriptome of restraint+PSD animals was enriched for microglia and macrophage proliferation, cellular response to corticosteroids, and apoptosis, among others. Finally, we identify sex-specific differences in restraint-induced genes following PSD. These findings provide genetic targets to consider when studying sleep and the response to stress. Frontiers Media S.A. 2019-10-09 /pmc/articles/PMC6794367/ /pubmed/31649619 http://dx.doi.org/10.3389/fendo.2019.00676 Text en Copyright © 2019 Oyola, Shupe, Soltis, Sukumar, Paez-Pereda, Larco, Wilkerson, Rothwell, Dalgard and Wu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Oyola, Mario G.
Shupe, Elizabeth A.
Soltis, Anthony R.
Sukumar, Gauthaman
Paez-Pereda, Marcelo
Larco, Darwin O.
Wilkerson, Matthew D.
Rothwell, Stephen
Dalgard, Clifton L.
Wu, T. John
Sleep Deprivation Alters the Pituitary Stress Transcriptome in Male and Female Mice
title Sleep Deprivation Alters the Pituitary Stress Transcriptome in Male and Female Mice
title_full Sleep Deprivation Alters the Pituitary Stress Transcriptome in Male and Female Mice
title_fullStr Sleep Deprivation Alters the Pituitary Stress Transcriptome in Male and Female Mice
title_full_unstemmed Sleep Deprivation Alters the Pituitary Stress Transcriptome in Male and Female Mice
title_short Sleep Deprivation Alters the Pituitary Stress Transcriptome in Male and Female Mice
title_sort sleep deprivation alters the pituitary stress transcriptome in male and female mice
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794367/
https://www.ncbi.nlm.nih.gov/pubmed/31649619
http://dx.doi.org/10.3389/fendo.2019.00676
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