Homeostatic crosstalk among gut microbiome, hypothalamic and hepatic circadian clock oscillations, immunity and metabolism in response to different light-dark cycles: A multiomics study
文献类型: 外文期刊
作者: Zhen, Yongkang 1 ; Wang, Yifan 1 ; He, Feiyang 1 ; Chen, Yifei 1 ; Hu, Liangyu 3 ; Ge, Ling 1 ; Wang, Yusu 1 ; Wei, Wenjun 1 ; Rahmat, Ali 1 ; Loor, Juan J. 4 ; Wang, Mengzhi 1 ;
作者机构: 1.Yangzhou Univ, Coll Anim Sci & Technol, Lab Metab Manipulat Herbivorous Anim Nutr, Yangzhou, Jiangsu, Peoples R China
2.Xinjiang Acad Agr Reclamat Sci, State Key Lab Sheep Genet Improvement & Hlth Prod, Shihezi, Xinjiang, Peoples R China
3.Wageningen Univ & Res, Human & Anim Physiol, Wageningen, Netherlands
4.Univ Illinois, Dept Anim Sci, Mammalian Nutr Physiol Genom, Urbana, IL USA
5.Univ Illinois, Div Nutr Sci, Urbana, IL USA
6.Yangzhou Univ, Coll Anim Sci & Technol, Lab Metab Manipulat Herbivorous Anim Nutr, Yangzhou 225009, Peoples R China
关键词: circadian clock; gut microbiome; host-microbes interaction; innate immune; light-dark cycles; tryptophan metabolism
期刊名称:JOURNAL OF PINEAL RESEARCH ( 影响因子:10.3; 五年影响因子:12.4 )
ISSN: 0742-3098
年卷期: 2023 年 75 卷 2 期
页码:
收录情况: SCI
摘要: The accelerated pace of life at present time has resulted in tremendous alterations in living patterns. Changes in diet and eating patterns, in particular, coupled with irregular light-dark (LD) cycles will further induce circadian misalignment and lead to disease. Emerging data has highlighted the regulatory effects of diet and eating patterns on the host-microbe interactions with the circadian clock (CC), immunity, and metabolism. Herein, we studied how LD cycles regulate the homeostatic crosstalk among the gut microbiome (GM), hypothalamic and hepatic CC oscillations, and immunity and metabolism using multiomics approaches. Our data demonstrated that central CC oscillations lost rhythmicity under irregular LD cycles, but LD cycles had minimal effects on diurnal expression of peripheral CC genes in the liver including Bmal1. We further demonstrated that the GM could regulate hepatic circadian rhythms under irregular LD cycles, the candidate bacteria including Limosilactobacillus, Actinomyces, Veillonella, Prevotella, Campylobacter, Faecalibacterium, Kingella, and Clostridia vadinBB60 et al. A comparative transcriptomic study of innate immune genes indicated that different LD cycles had varying effects on immune functions, while irregular LD cycles had greater impacts on hepatic innate immune functions than those in the hypothalamus. Extreme LD cycle alterations (LD0/24 and LD24/0) had worse impacts than slight alterations (LD8/16 and LD16/8), and led to gut dysbiosis in mice receiving antibiotics. Metabolome data also demonstrated that hepatic tryptophan metabolism mediated the homeostatic crosstalk among GM-liver-brain axis in response to different LD cycles. These research findings highlighted that GM could regulate immune and metabolic disorders induced by circadian dysregulation. Further, the data provided potential targets for developing probiotics for individuals with circadian disruption such as shift workers.
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