Circadian Clock Proteins and Immunity

被引:555
作者
Curtis, Anne M. [1 ]
Bellet, Marina M. [2 ]
Sassone-Corsi, Paolo [2 ]
O'Neill, Luke A. J. [1 ]
机构
[1] Univ Dublin Trinity Coll, Trinity Biomed Sci Inst, Sch Biochem & Immunol, Dublin 2, Ireland
[2] Univ Calif Irvine, Dept Biol Chem, Ctr Epigenet & Metab, Irvine, CA 92697 USA
基金
欧洲研究理事会;
关键词
REV-ERB-ALPHA; GENE-EXPRESSION; SHIFT-WORK; NEGATIVE REGULATOR; INNATE IMMUNITY; HOST RESPONSE; RECEPTOR; RHYTHMS; METABOLISM; SUSCEPTIBILITY;
D O I
10.1016/j.immuni.2014.02.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Immune parameters change with time of day and disruption of circadian rhythms has been linked to inflammatory pathologies. A circadian-clock-controlled immune system might allow an organism to anticipate daily changes in activity and feeding and the associated risk of infection or tissue damage to the host. Responses to bacteria have been shown to vary depending on time of infection, with mice being more at risk of sepsis when challenged ahead of their activity phase. Studies highlight the extent to which the molecular clock, most notably the core clock proteins BMAL1, CLOCK, and REV-ERB alpha, control fundamental aspects of the immune response. Examples include the BMAL1: CLOCK heterodimer regulating toll-like receptor 9 (TLR9) expression and repressing expression of the inflammatory monocyte chemokine ligand (CCL2) as well as REV-ERBa suppressing the induction of interleukin-6. Understanding the daily rhythm of the immune system could have implications for vaccinations and how we manage infectious and inflammatory diseases.
引用
收藏
页码:178 / 186
页数:9
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