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Gut Microbiome-Related Anti-Inflammatory Effects of Aryl Hydrocarbon Receptor Activation on Inflammatory Bowel Disease
被引:1
作者:
Moutusy, Salvinaz Islam
[1
,2
,3
]
Ohsako, Seiichiroh
[1
]
机构:
[1] Univ Tokyo, Ctr Dis Biol & Integrat Med, Grad Sch Med, Lab Environm Hlth Sci, Tokyo 1130033, Japan
[2] Stanford Univ, Dept Med, Div Immunol & Rheumatol, Stanford, CA 94305 USA
[3] VA Palo Alto Hlth Care Syst, Palo Alto, CA 94305 USA
基金:
日本学术振兴会;
关键词:
inflammatory bowel diseases (IBD);
aryl hydrocarbon receptor (AHR);
gut microbiota;
inflammation;
dysbiosis;
REGULATORY T-CELLS;
GROWTH-FACTOR-BETA;
ULCERATIVE-COLITIS;
INTESTINAL MICROBIOTA;
DENDRITIC CELLS;
EPITHELIAL-CELLS;
BARRIER FUNCTION;
CROHNS-DISEASE;
TH17;
CELLS;
DIFFERENTIATION;
D O I:
10.3390/ijms25063372
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Inflammatory bowel disease (IBD) is one of the most prevalent chronic inflammations of the gastrointestinal tract (GIT). The gut microbial population, the cytokine milieu, the aryl hydrocarbon receptor (AHR) expressed by immune and nonimmune cells and the intrinsic pathway of Th-cell differentiation are implicated in the immunopathology of IBD. AHR activation requires a delicate balance between regulatory and effector T-cells; loss of this balance can cause local gut microbial dysbiosis and intestinal inflammation. Thus, the study of the gut microbiome in association with AHR provides critical insights into IBD pathogenesis and interventions. This review will focus on the recent advancements to form conceptional frameworks on the benefits of AHR activation by commensal gut bacteria in IBD.
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