The cross talk between microbiota and the immune system: metabolites take center stage

被引:140
作者
Shapiro, Hagit [1 ]
Thaiss, Christoph A. [1 ]
Levy, Maayan [1 ]
Elinav, Eran [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
基金
欧洲研究理事会;
关键词
CONJUGATED LINOLEIC-ACID; ARYL-HYDROCARBON RECEPTOR; FARNESOID X RECEPTOR; NF-KAPPA-B; VITAMIN-A; GUT MICROBIOTA; RETINOIC ACID; PPAR-GAMMA; CELL PROLIFERATION; DENDRITIC CELLS;
D O I
10.1016/j.coi.2014.07.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The human meta-organism consists of more than 90% of microbial cells. The gastrointestinal tract harbors trillions of commensal microorganisms that influence the development and homeostasis of the host. Alterations in composition and function of the microbiota, termed dysbiosis, have been implicated in a multitude of metabolic and inflammatory diseases in humans. Thus, understanding the molecular underpinnings the cross talk between commensal bacteria and their host during homeostasis and dysbiosis may hold the key to understanding many idiopathic diseases. While most attention has focused on the innate recognition of immune-stimulatory bacterial molecules, such as cell wall components and nucleic acids, we emphasize here the impact of diet-dependent microbial metabolites on the development and function of the immune system.
引用
收藏
页码:54 / 62
页数:9
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