孕烷X受体
TLR4型
生物
下调和上调
细胞生物学
核受体
受体
Toll样受体
信号转导
肠细胞
促炎细胞因子
肠粘膜
生物化学
转录因子
炎症
先天免疫系统
免疫学
基因
小肠
内科学
医学
作者
Madhukumar Venkatesh,Subhajit Mukherjee,Hongwei Wang,Hao Li,Katherine Sun,Alexandre P. Bénéchet,Zhijuan Qiu,Leigh Maher,Matthew R. Redinbo,Bob Phillips,James C. Fleet,Sandhya Kortagere,Paromita Mukherjee,Alessio Fasano,Jessica Le Ven,Jeremy K. Nicholson,Marc Dumas,Kamal M. Khanna,Sridhar Mani
出处
期刊:Immunity
[Elsevier]
日期:2014-08-01
卷期号:41 (2): 296-310
被引量:723
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.
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