| Literature DB >> 36266581 |
Liliana M Sanmarco1, Chun-Cheih Chao1, Yu-Chao Wang2, Jessica E Kenison1, Zhaorong Li1, Joseph M Rone1, Claudia M Rejano-Gordillo1, Carolina M Polonio1, Cristina Gutierrez-Vazquez1, Gavin Piester1,3, Agustin Plasencia1, Lucinda Li1, Federico Giovannoni1, Hong-Gyun Lee1, Camilo Faust Akl1, Michael A Wheeler1,4, Ivan Mascanfroni1, Merja Jaronen1, Moneera Alsuwailm1, Patrick Hewson1, Ada Yeste1, Brian M Andersen1,5, Diana G Franks6, Chien-Jung Huang2, Millicent Ekwudo1, Emily C Tjon1, Veit Rothhammer1, Maisa Takenaka1, Kalil Alves de Lima1, Mathias Linnerbauer1, Lydia Guo1, Ruxandra Covacu1, Hugo Queva1, Pedro Henrique Fonseca-Castro1, Maha Al Bladi1, Laura M Cox1, Kevin J Hodgetts1, Mark E Hahn6, Alexander Mildner7, Joshua Korzenik8, Russ Hauser9, Scott B Snapper10,11, Francisco J Quintana12,13.
Abstract
Genome-wide association studies have identified risk loci linked to inflammatory bowel disease (IBD)1-a complex chronic inflammatory disorder of the gastrointestinal tract. The increasing prevalence of IBD in industrialized countries and the augmented disease risk observed in migrants who move into areas of higher disease prevalence suggest that environmental factors are also important determinants of IBD susceptibility and severity2. However, the identification of environmental factors relevant to IBD and the mechanisms by which they influence disease has been hampered by the lack of platforms for their systematic investigation. Here we describe an integrated systems approach, combining publicly available databases, zebrafish chemical screens, machine learning and mouse preclinical models to identify environmental factors that control intestinal inflammation. This approach established that the herbicide propyzamide increases inflammation in the small and large intestine. Moreover, we show that an AHR-NF-κB-C/EBPβ signalling axis operates in T cells and dendritic cells to promote intestinal inflammation, and is targeted by propyzamide. In conclusion, we developed a pipeline for the identification of environmental factors and mechanisms of pathogenesis in IBD and, potentially, other inflammatory diseases.Entities:
Year: 2022 PMID: 36266581 DOI: 10.1038/s41586-022-05308-6
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 69.504