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Day–night fluctuations in choroid plexus transcriptomics and cerebrospinal fluid metabolomics

The cerebrospinal fluid (CSF) provides mechanical protection for the brain and serves as a brain dispersion route for nutrients, hormones, and metabolic waste. The CSF secretion rate is elevated in the dark phase in both humans and rats, which could support the CSF flow along the paravascular spaces...

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Autores principales: Edelbo, Beatriche Louise, Andreassen, Søren Norge, Steffensen, Annette Buur, MacAulay, Nanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443925/
https://www.ncbi.nlm.nih.gov/pubmed/37614671
http://dx.doi.org/10.1093/pnasnexus/pgad262
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author Edelbo, Beatriche Louise
Andreassen, Søren Norge
Steffensen, Annette Buur
MacAulay, Nanna
author_facet Edelbo, Beatriche Louise
Andreassen, Søren Norge
Steffensen, Annette Buur
MacAulay, Nanna
author_sort Edelbo, Beatriche Louise
collection PubMed
description The cerebrospinal fluid (CSF) provides mechanical protection for the brain and serves as a brain dispersion route for nutrients, hormones, and metabolic waste. The CSF secretion rate is elevated in the dark phase in both humans and rats, which could support the CSF flow along the paravascular spaces that may be implicated in waste clearance. The similar diurnal CSF dynamics pattern observed in the day-active human and the nocturnal rat suggests a circadian regulation of this physiological variable, rather than sleep itself. To obtain a catalog of potential molecular drivers that could provide the day–night-associated modulation of the CSF secretion rate, we determined the diurnal fluctuation in the rat choroid plexus transcriptomic profile with RNA-seq and in the CSF metabolomics with ultraperformance liquid chromatography combined with mass spectrometry. We detected significant fluctuation of 19 CSF metabolites and differential expression of 2,778 choroid plexus genes between the light and the dark phase, the latter of which encompassed circadian rhythm–related genes and several choroid plexus transport mechanisms. The fluctuating components were organized with joint pathway analysis, of which several pathways demonstrated diurnal regulation. Our results illustrate substantial transcriptional and metabolic light–dark phase–mediated changes taking place in the rat choroid plexus and its encircling CSF. The combined data provide directions toward future identification of the molecular pathways governing the fluctuation of this physiological process and could potentially be harnessed to modulate the CSF dynamics in pathology.
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spelling pubmed-104439252023-08-23 Day–night fluctuations in choroid plexus transcriptomics and cerebrospinal fluid metabolomics Edelbo, Beatriche Louise Andreassen, Søren Norge Steffensen, Annette Buur MacAulay, Nanna PNAS Nexus Biological, Health, and Medical Sciences The cerebrospinal fluid (CSF) provides mechanical protection for the brain and serves as a brain dispersion route for nutrients, hormones, and metabolic waste. The CSF secretion rate is elevated in the dark phase in both humans and rats, which could support the CSF flow along the paravascular spaces that may be implicated in waste clearance. The similar diurnal CSF dynamics pattern observed in the day-active human and the nocturnal rat suggests a circadian regulation of this physiological variable, rather than sleep itself. To obtain a catalog of potential molecular drivers that could provide the day–night-associated modulation of the CSF secretion rate, we determined the diurnal fluctuation in the rat choroid plexus transcriptomic profile with RNA-seq and in the CSF metabolomics with ultraperformance liquid chromatography combined with mass spectrometry. We detected significant fluctuation of 19 CSF metabolites and differential expression of 2,778 choroid plexus genes between the light and the dark phase, the latter of which encompassed circadian rhythm–related genes and several choroid plexus transport mechanisms. The fluctuating components were organized with joint pathway analysis, of which several pathways demonstrated diurnal regulation. Our results illustrate substantial transcriptional and metabolic light–dark phase–mediated changes taking place in the rat choroid plexus and its encircling CSF. The combined data provide directions toward future identification of the molecular pathways governing the fluctuation of this physiological process and could potentially be harnessed to modulate the CSF dynamics in pathology. Oxford University Press 2023-08-10 /pmc/articles/PMC10443925/ /pubmed/37614671 http://dx.doi.org/10.1093/pnasnexus/pgad262 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of National Academy of Sciences. 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 Biological, Health, and Medical Sciences
Edelbo, Beatriche Louise
Andreassen, Søren Norge
Steffensen, Annette Buur
MacAulay, Nanna
Day–night fluctuations in choroid plexus transcriptomics and cerebrospinal fluid metabolomics
title Day–night fluctuations in choroid plexus transcriptomics and cerebrospinal fluid metabolomics
title_full Day–night fluctuations in choroid plexus transcriptomics and cerebrospinal fluid metabolomics
title_fullStr Day–night fluctuations in choroid plexus transcriptomics and cerebrospinal fluid metabolomics
title_full_unstemmed Day–night fluctuations in choroid plexus transcriptomics and cerebrospinal fluid metabolomics
title_short Day–night fluctuations in choroid plexus transcriptomics and cerebrospinal fluid metabolomics
title_sort day–night fluctuations in choroid plexus transcriptomics and cerebrospinal fluid metabolomics
topic Biological, Health, and Medical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443925/
https://www.ncbi.nlm.nih.gov/pubmed/37614671
http://dx.doi.org/10.1093/pnasnexus/pgad262
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