免疫系统
法尼甾体X受体
肠道菌群
菌群(微生物学)
生物
G蛋白偶联胆汁酸受体
胆汁酸
受体
肿瘤微环境
免疫学
核受体
生物化学
细菌
转录因子
遗传学
基因
作者
Yan Zhang,Xueyan Gao,Feng Yang,Yang Liu,Shuochen Gao,Liping Pei,Wenkang Wang,Zhenqiang Sun,Lin Liu,Chengzeng Wang
出处
期刊:Authorea - Authorea
日期:2023-03-07
标识
DOI:10.22541/au.167820161.17527231/v1
摘要
According to reports, gut microbiota and metabolites regulate intestinal immune microenvironment. In recent years, an increasing number of studies reported that bile acids (BAs) of intestinal flora origin affects T helper cells and Treg cells. Th17 cells play a pro-inflammatory role and Treg cells usually act an immunosuppressive role. In this review, we emphatically summarized the influence and corresponding mechanism of different configurations of the LCA and DCA on intestinal Th17 cells, Treg cells and intestinal immune microenvironment. The regulation of BAs receptors G protein-coupled bile acid receptor 1 (GPBAR1/TGR5) and farnesoid X receptor (FXR) on immune cells and intestinal environment are elaborated. Furthermore, the potential clinical applications above were also concluded in three aspects. These above will help researchers better understand the effects of gut flora on the intestinal immune microenvironment via BAs and contribute to the development of new targeted drugs.
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