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Plasma and cerebrospinal fluid proteomic signatures of acutely sleep-deprived humans: an exploratory study

STUDY OBJECTIVES: Acute sleep deprivation affects both central and peripheral biological processes. Prior research has mainly focused on specific proteins or biological pathways that are dysregulated in the setting of sustained wakefulness. This exploratory study aimed to provide a comprehensive vie...

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Autores principales: Vaquer-Alicea, Ana, Yu, Jinsheng, Liu, Haiyan, Lucey, Brendan P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10691441/
https://www.ncbi.nlm.nih.gov/pubmed/38046221
http://dx.doi.org/10.1093/sleepadvances/zpad047
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author Vaquer-Alicea, Ana
Yu, Jinsheng
Liu, Haiyan
Lucey, Brendan P
author_facet Vaquer-Alicea, Ana
Yu, Jinsheng
Liu, Haiyan
Lucey, Brendan P
author_sort Vaquer-Alicea, Ana
collection PubMed
description STUDY OBJECTIVES: Acute sleep deprivation affects both central and peripheral biological processes. Prior research has mainly focused on specific proteins or biological pathways that are dysregulated in the setting of sustained wakefulness. This exploratory study aimed to provide a comprehensive view of the biological processes and proteins impacted by acute sleep deprivation in both plasma and cerebrospinal fluid (CSF). METHODS: We collected plasma and CSF from human participants during one night of sleep deprivation and controlled normal sleep conditions. One thousand and three hundred proteins were measured at hour 0 and hour 24 using a high-scale aptamer-based proteomics platform (SOMAscan) and a systematic biological database tool (Metascape) was used to reveal altered biological pathways. RESULTS: Acute sleep deprivation decreased the number of upregulated and downregulated biological pathways and proteins in plasma but increased upregulated and downregulated biological pathways and proteins in CSF. Predominantly affected proteins and pathways were associated with immune response, inflammation, phosphorylation, membrane signaling, cell-cell adhesion, and extracellular matrix organization. CONCLUSIONS: The identified modifications across biofluids add to evidence that acute sleep deprivation has important impacts on biological pathways and proteins that can negatively affect human health. As a hypothesis-driving study, these findings may help with the exploration of novel mechanisms that mediate sleep loss and associated conditions, drive the discovery of new sleep loss biomarkers, and ultimately aid in the identification of new targets for intervention to human diseases.
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spelling pubmed-106914412023-12-02 Plasma and cerebrospinal fluid proteomic signatures of acutely sleep-deprived humans: an exploratory study Vaquer-Alicea, Ana Yu, Jinsheng Liu, Haiyan Lucey, Brendan P Sleep Adv Original Article STUDY OBJECTIVES: Acute sleep deprivation affects both central and peripheral biological processes. Prior research has mainly focused on specific proteins or biological pathways that are dysregulated in the setting of sustained wakefulness. This exploratory study aimed to provide a comprehensive view of the biological processes and proteins impacted by acute sleep deprivation in both plasma and cerebrospinal fluid (CSF). METHODS: We collected plasma and CSF from human participants during one night of sleep deprivation and controlled normal sleep conditions. One thousand and three hundred proteins were measured at hour 0 and hour 24 using a high-scale aptamer-based proteomics platform (SOMAscan) and a systematic biological database tool (Metascape) was used to reveal altered biological pathways. RESULTS: Acute sleep deprivation decreased the number of upregulated and downregulated biological pathways and proteins in plasma but increased upregulated and downregulated biological pathways and proteins in CSF. Predominantly affected proteins and pathways were associated with immune response, inflammation, phosphorylation, membrane signaling, cell-cell adhesion, and extracellular matrix organization. CONCLUSIONS: The identified modifications across biofluids add to evidence that acute sleep deprivation has important impacts on biological pathways and proteins that can negatively affect human health. As a hypothesis-driving study, these findings may help with the exploration of novel mechanisms that mediate sleep loss and associated conditions, drive the discovery of new sleep loss biomarkers, and ultimately aid in the identification of new targets for intervention to human diseases. Oxford University Press 2023-11-14 /pmc/articles/PMC10691441/ /pubmed/38046221 http://dx.doi.org/10.1093/sleepadvances/zpad047 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Sleep Research Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Vaquer-Alicea, Ana
Yu, Jinsheng
Liu, Haiyan
Lucey, Brendan P
Plasma and cerebrospinal fluid proteomic signatures of acutely sleep-deprived humans: an exploratory study
title Plasma and cerebrospinal fluid proteomic signatures of acutely sleep-deprived humans: an exploratory study
title_full Plasma and cerebrospinal fluid proteomic signatures of acutely sleep-deprived humans: an exploratory study
title_fullStr Plasma and cerebrospinal fluid proteomic signatures of acutely sleep-deprived humans: an exploratory study
title_full_unstemmed Plasma and cerebrospinal fluid proteomic signatures of acutely sleep-deprived humans: an exploratory study
title_short Plasma and cerebrospinal fluid proteomic signatures of acutely sleep-deprived humans: an exploratory study
title_sort plasma and cerebrospinal fluid proteomic signatures of acutely sleep-deprived humans: an exploratory study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10691441/
https://www.ncbi.nlm.nih.gov/pubmed/38046221
http://dx.doi.org/10.1093/sleepadvances/zpad047
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