孕烷X受体
异型生物质的
生物
细胞生物学
功能(生物学)
核受体
受体
Toll样受体
伤亡人数
势垒函数
微生物学
计算生物学
生物化学
转录因子
先天免疫系统
免疫学
基因
酶
作者
Madhukumar Venkatesh,Subhajit Mukherjee,Hongwei Wang,Hao Li,Katherine Sun,Alexandre P. Bénéchet,Zhijuan Qiu,Leigh Maher,Matthew R. Redinbo,Robert S. Phillips,James C. Fleet,Sandhya Kortagere,Paromita Mukherjee,Alessio Fasano,Jessica Le Ven,Jeremy K. Nicholson,Marc‐Emmanuel Dumas,Kamal M. Khanna,Sridhar Mani
出处
期刊:Immunity
[Cell Press]
日期:2014-07-24
卷期号:41 (2): 296-310
被引量:838
标识
DOI:10.1016/j.immuni.2014.06.014
摘要
Intestinal microbial metabolites are conjectured to affect mucosal integrity through an incompletely characterized mechanism. Here we showed that microbial-specific indoles regulated intestinal barrier function through the xenobiotic sensor, pregnane X receptor (PXR). Indole 3-propionic acid (IPA), in the context of indole, is a ligand for PXR in vivo, and IPA downregulated enterocyte TNF-α while it upregulated junctional protein-coding mRNAs. PXR-deficient (Nr1i2(-/-)) mice showed a distinctly "leaky" gut physiology coupled with upregulation of the Toll-like receptor (TLR) signaling pathway. These defects in the epithelial barrier were corrected in Nr1i2(-/-)Tlr4(-/-) mice. Our results demonstrate that a direct chemical communication between the intestinal symbionts and PXR regulates mucosal integrity through a pathway that involves luminal sensing and signaling by TLR4.
科研通智能强力驱动
Strongly Powered by AbleSci AI