Aryl hydrocarbon receptor and intestinal immunity

被引:396
作者
Lamas, Bruno [1 ,2 ]
Natividad, Jane M. [2 ]
Sokol, Harry [1 ,2 ]
机构
[1] PSL Res Univ, Sorbonne Univ, Ecole Normale Super, LBM,CNRS,INSERM,Hop St Antoine,AP HP,Lab Biomol, F-75005 Paris, France
[2] Univ Paris Saclay, Micalis Inst, INRA, AgroParisTech, F-78350 Jouy En Josas, France
基金
欧洲研究理事会;
关键词
TUMOR-SUPPRESSOR GENE; LIVER-CELL CULTURE; REGULATORY T-CELLS; NF-KAPPA-B; AH RECEPTOR; DIOXIN RECEPTOR; NUCLEAR TRANSLOCATOR; IL-22; PRODUCTION; DENDRITIC CELLS; GUT MICROBIOTA;
D O I
10.1038/s41385-018-0019-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aryl hydrocarbon receptor (AhR) is a member of the basic helix-loop-helix-(bHLH) superfamily of transcription factors, which are associated with cellular responses to environmental stimuli, such as xenobiotics and oxygen levels. Unlike other members of bHLH, AhR is the only bHLH transcription factor that is known to be ligand activated. Early AhR studies focused on understanding the role of AhR in mediating the toxicity and carcinogenesis properties of the prototypic ligand 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). In recent years, however, it has become apparent that, in addition to its toxicological involvement, AhR is highly receptive to a wide array of endogenous and exogenous ligands, and that its activation leads to a myriad of key host physiological functions. In this study, we review the current understanding of the functions of AhR in the mucosal immune system with a focus on its role in intestinal barrier function and intestinal immune cells, as well as in intestinal homeostasis.
引用
收藏
页码:1024 / 1038
页数:15
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