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IL-6 decodes sex and diet-dependent circadian and metabolic rhythms

Gonzalez-Vila, Antia; Ibrahim-Alasoufi, Ali Mohammad; Luengo-Mateos, Maria; Pardo-Garcia, Victor; Diaz-Lopez, Alejandro; Fernandez-Rodriguez, Belen; Poutanen, Matti; Ohlsson, Claes; Tena-Sempere, Manuel; Dieguez-Gonzalez, Carlos; Garcia-Garcia; Maria del Carmen; Barca-Mayo, Olga

IL-6 decodes sex and diet-dependent circadian and metabolic rhythms

Gonzalez-Vila, Antia
Ibrahim-Alasoufi, Ali Mohammad
Luengo-Mateos, Maria
Pardo-Garcia, Victor
Diaz-Lopez, Alejandro
Fernandez-Rodriguez, Belen
Poutanen, Matti
Ohlsson, Claes
Tena-Sempere, Manuel
Dieguez-Gonzalez, Carlos
Garcia-Garcia
Maria del Carmen
Barca-Mayo, Olga
Katso/Avaa
1-s2.0-S221287782500078X-main.pdf (4.914Mb)
Lataukset: 

Elsevier BV
doi:10.1016/j.molmet.2025.102171
URI
https://doi.org/10.1016/j.molmet.2025.102171
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2025082792850
Tiivistelmä

Objective: Interleukin-6 (IL-6) is a pleiotropic cytokine involved in immune regulation and energy metabolism. Its diurnal secretion influences core circadian components, emphasizing its critical role in circadian biology. Despite known sex differences in immune, circadian, and metabolic processes, how IL-6 integrates these processes remains poorly understood.

Methods: IL6 knockout (KO) and control mice of both sexes were phenotyped for circadian and metabolic traits under standard (STD) and high-fat diet (HFD), fasting, and time-restricted feeding. Molecular analyses in muscle, liver, and hypothalamus assessed clock gene expression and IL-6 signaling pathway. Circulating sex steroid hormones were quantified to examine their contribution to the observed sex-specific phenotypes.

Results: IL-6 deficiency disrupts circadian locomotor and metabolic rhythms in a sex- and diet-dependent manner. Males exhibit impaired light-driven circadian rhythms under STD conditions and metabolic misalignment under HFD, whereas females display greater circadian resilience under STD conditions but increased vulnerability to circadian disruption during HFD. Additionally, IL-6 emerges as a novel regulator of the food-entrainable oscillator (FEO), linking food anticipatory activity and metabolic cycles under both STD and HFD in a sex-dependent manner.

Conclusions: These findings identify IL-6 as a critical mediator of circadian-metabolic plasticity, shaping sex- and diet-specific trade-offs between circadian stability and metabolic homeostasis. Our study highlights IL-6 as a potential therapeutic target for mitigating circadian misalignment-associated metabolic disorders, with implications for the timed modulation of IL-6 signaling.

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