Regulatory Effects of Clock and Bmal1 on Circadian Rhythmic TLR Expression

被引:8
作者
Fan, Xu-li [1 ]
Song, Ying [1 ]
Qin, Dong-Xu [1 ]
Lin, Pei-Yao [1 ]
机构
[1] Zhejiang Univ Technol, Dept Pharmacol, 18 Chao Wang Rd, Hangzhou 310014, Zhejiang, Peoples R China
关键词
Clock; Bmal1; Circadian clock; Toll-like receptors; Circadian rhythm; TOLL-LIKE RECEPTORS; GENE-EXPRESSION; INNATE IMMUNITY; SIGNALING PATHWAYS; SKIN INFLAMMATION; DENDRITIC CELLS; PROTEIN; METABOLISM; ATHEROSCLEROSIS; IDENTIFICATION;
D O I
10.1080/08830185.2021.1931170
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Circadian locomotor output cycles kaput (Clock) and brain and muscle ARNT-like 1 (Bmal1) are two core circadian clock genes. They form a heterodimer that can bind to the E-box element in the promoters of Period circadian protein (Per) and Cryptochrome (Cry) genes, thereby inducing the rhythmic expression of circadian clock control genes. Toll-like receptors (TLRs) are type I transmembrane proteins belonging to the pattern recognition receptor (PRR) family. They can recognize a variety of pathogens and play an important role in innate immunity and adaptive immune responses. Recent studies have found that the circadian clock is closely associated with the immune system. TLRs have a certain correlation with the circadian rhythms; Bmal1 seems to be the central mediator connecting the circadian clock and the immune system. Research on Bmal1 and TLRs has made some progress, but the specific relationship between TLRs and Bmal1 remains unclear. Understanding the relationship between TLRs and Clock/Bmal1 genes is increasingly important for basic research and clinical treatment.
引用
收藏
页码:101 / 112
页数:12
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