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Feeding regime synchronizes circadian clock in choroid plexus insight into a complex mechanism

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985823%3A_____%2F25%3A00637055" target="_blank" >RIV/67985823:_____/25:00637055 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11130/25:10499322 RIV/00216208:11310/25:10499322

  • Result on the web

    <a href="https://doi.org/10.1007/s00018-025-05798-3" target="_blank" >https://doi.org/10.1007/s00018-025-05798-3</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00018-025-05798-3" target="_blank" >10.1007/s00018-025-05798-3</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Feeding regime synchronizes circadian clock in choroid plexus insight into a complex mechanism

  • Original language description

    The circadian clock in choroid plexus (ChP) controls processes involved in its physiological functions, but the signals that synchronize the clock have been sparsely studied. We found that the ChP clock in the fourthventricle (4V) is more robust than that in the lateral ventricle (LV) and investigated whether both clocks use information about mealtime as a signal to synchronize with the current activity state. Exposure of mPer2Luc mice to a 10-day reverse restricted feeding (rRF) protocol, in which food was provided for 6 h during daytime, advanced the phase of the ChP clock in 4V and LV, as evidenced by shifted (1) PER2-driven bioluminescence rhythms of ChP explants ex vivo and (2) daily profiles in clock gene expression in both ChP tissues in vivo. In contrast, clocks in other brain regions (DMH, ARC, LHb) of the same mice did not shift. The 4V ChP responded more strongly than the LV ChP to rRF by modulating the expression of genes to ensure a decrease in resistance to cerebrospinal fluid drainage and increase the secretory capacity of ChP cells. Mechanistically, rRF affects the ChP clock through food-induced increases in insulin, glucose and temperature levels, as in vitro all three signals significantly shifted the clocks in both ChP tissues, similar to rRF. The effect of glucose was partially blocked by OSMI-1, suggesting involvement of O-linked N-acetylglucosamine posttranslational modification. We identified mechanisms that can signal to the brain the time of feeding and the associated activity state via resetting of the ChP clock.Graphical abstractSummary of results. Reverse restricted feeding (rRF), which shifts the timing of food intake into the daytime, leads to a corresponding shift in the rise of insulin and glucose levels as well as activity-related body temperature. As a result, the clocks in the choroid plexus of the fourth ventricle (4V ChP) and the lateral ventricle (LV ChP) shift accordingly (the effect of glucose is partly mediated via O-GlcNAcylation). In this way, clock-controlled ChP function follows the timing of food rather than solar cycle.

  • 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

    30105 - Physiology (including cytology)

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

    2025

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Cellular and Molecular Life Sciences

  • ISSN

    1420-682X

  • e-ISSN

    1420-9071

  • Volume of the periodical

    82

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    18

  • Pages from-to

    247

  • UT code for WoS article

    001513968700001

  • EID of the result in the Scopus database

    2-s2.0-105008808482