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Circadian clock in choroid plexus is resistant to immune challenge but dampens in response to chronodisruption

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985823%3A_____%2F24%3A00583226" target="_blank" >RIV/67985823:_____/24:00583226 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1016/j.bbi.2024.01.217" target="_blank" >https://doi.org/10.1016/j.bbi.2024.01.217</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.bbi.2024.01.217" target="_blank" >10.1016/j.bbi.2024.01.217</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Circadian clock in choroid plexus is resistant to immune challenge but dampens in response to chronodisruption

  • Original language description

    The choroid plexus (ChP) in the brain ventricles has a major influence on brain homeostasis. In this study, we aimed to determine whether the circadian clock located in ChP is affected by chronodisruption caused by misalignment with the external light/dark cycle and/or inflammation. Adult mPer2Luc mice were maintained in the LD12:12 cycle or exposed to one of two models of chronic chronodisruption – constant light for 22–25 weeks (cLL) or 6-hour phase advances of the LD12:12 cycle repeated weekly for 12 weeks (cLD-shifts). Locomotor activity was monitored before the 4th ventricle ChP and suprachiasmatic nuclei (SCN) explants were recorded in real time for PER2-driven population and single-cell bioluminescence rhythms. In addition, plasma immune marker concentrations and gene expression in ChP, prefrontal cortex, hippocampus and cerebellum were analyzed. cLL dampened the SCN clock but did not shorten the inactivity interval (sleep). cLD-shifts had no effect on the SCN clock, but transiently affected sleep duration and fragmentation. Both chronodisruption protocols dampened the ChP clock. Although immune markers were elevated in plasma and hippocampus, levels in ChP were unaffected, and unlike the liver clock, the ChP clock was resistant to lipopolysaccharide treatment. Importantly, both chronodisruption protocols reduced glucocorticoid signaling in ChP. The data demonstrate the high resistance of the ChP clock to inflammation, highlighting its role in protecting the brain from neuroinflammation, and on the other hand its high sensitivity to chronodisruption. Our results provide a novel link between human lifestyle-induced chronodisruption and the impairment of ChP-dependent brain homeostasis.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30103 - Neurosciences (including psychophysiology)

Result continuities

  • Project

    <a href="/en/project/GA21-09745S" target="_blank" >GA21-09745S: Circadian clock in choroid plexus and its sensitivity to chronodisruption and neuroinflammation</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Brain Behavior and Immunity

  • ISSN

    0889-1591

  • e-ISSN

    1090-2139

  • Volume of the periodical

    117

  • Issue of the periodical within the volume

    March

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    15

  • Pages from-to

    255-269

  • UT code for WoS article

    001174463800001

  • EID of the result in the Scopus database

    2-s2.0-85183961992