Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Subscribe

Sci. STKE, 7 August 2007
Vol. 2007, Issue 398, p. tw280
[DOI: 10.1126/stke.3982007tw280]

EDITORS' CHOICE

Circadian Rhythms Sleepy Time with TNF-{alpha}

John F. Foley

Science’s STKE, AAAS, Washington, DC 20005, USA

Why is it that soon after being exposed to an infectious agent we suffer from fatigue as well as fever? Part of the innate immune response to microbial infections is the production of proinflammatory cytokines such as interleukin (IL)-1beta and tumor necrosis factor-{alpha} (TNF-{alpha}). Previous studies have implicated TNF-{alpha} as a causative agent of fatigue in humans and mice; however, the mechanism is not known. Sleep is regulated by circadian mechanisms that include a negative feedback system involving the Per transcriptional repressors, the abundance of which is controlled by the transcription factors BMAL1 and CLOCK, whose expression is in turn controlled by the Per repressors. Cavadini et al. treated synchronized NIH 3T3 fibroblasts with TNF-{alpha} and observed a dose-dependent decrease in the expression of the transcriptional repressor genes Per1, Per2, and Per3 compared with untreated cells, as assessed by real-time reverse transcription polymerase chain reaction (RT-PCR) analyses. The effect of TNF-{alpha} on Per gene expression was shared by IL-1beta but not by interferon-{alpha} (IFN-{alpha}) or IL-6, two other proinflammatory cytokines that are produced upon microbial infection. Clock gene expression was unaffected by TNF-{alpha} treatment. Using fibroblasts transfected with luciferase reporter genes, the authors demonstrated that TNF-{alpha} treatment inhibited expression of circadian genes under the control of promoters that contained an E-box motif--a helix-loop-helix transcription factor-binding site. Per genes, which were inhibited by TNF-{alpha}, contain E-box motifs, whereas Bmal1 and Clock genes, which were not affected by TNF-{alpha}, do not. Mice were treated with TNF-{alpha} every day for 7 days, and RT-PCR analysis of the liver showed decreased expression of Per3 and other genes regulated by circadian processes, such as Dbp, which encodes the transcription factor Dbp that contributes to circadian control of locomotor activity. TNF-{alpha} treatment of mice also decreased Dbp expression in the hypothalamus. By monitoring running-wheel activity, Cavadini et al. showed that administration of TNF-{alpha} to mice reduced their movements and increased the amount of time that the mice spent resting. Together, these data suggest that TNF-{alpha}, produced during the initial stages of microbial infections and associated with autoimmune disorders such as rheumatoid arthritis, alters circadian signaling and induces fatigue. Clinical intervention to prevent this may help patients overcome the disruptive effects of TNF-{alpha} on their sleep patterns.

G. Cavadini, S. Petrzilka, P. Kohler, C. Jud, I. Tobler, T. Birchler, A. Fontana, TNF-{alpha} suppresses the expression of clock genes by interfering with E-box-mediated transcription. Proc. Natl. Acad. Sci. U.S.A. 104, 12843-12848 (2007). [Abstract] [Full Text]

Citation: J. F. Foley, Sleepy Time with TNF-{alpha}. Sci. STKE 2007, tw280 (2007).



To Advertise     Find Products


Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882