TY - JOUR
T1 - Identification of environmental factors that promote intestinal inflammation
AU - Sanmarco, Liliana M.
AU - Chao, Chun Cheih
AU - Wang, Yu Chao
AU - Kenison, Jessica E.
AU - Li, Zhaorong
AU - Rone, Joseph M.
AU - Rejano-Gordillo, Claudia M.
AU - Polonio, Carolina M.
AU - Gutierrez-Vazquez, Cristina
AU - Piester, Gavin
AU - Plasencia, Agustin
AU - Li, Lucinda
AU - Giovannoni, Federico
AU - Lee, Hong Gyun
AU - Faust Akl, Camilo
AU - Wheeler, Michael A.
AU - Mascanfroni, Ivan
AU - Jaronen, Merja
AU - Alsuwailm, Moneera
AU - Hewson, Patrick
AU - Yeste, Ada
AU - Andersen, Brian M.
AU - Franks, Diana G.
AU - Huang, Chien Jung
AU - Ekwudo, Millicent
AU - Tjon, Emily C.
AU - Rothhammer, Veit
AU - Takenaka, Maisa
AU - de Lima, Kalil Alves
AU - Linnerbauer, Mathias
AU - Guo, Lydia
AU - Covacu, Ruxandra
AU - Queva, Hugo
AU - Fonseca-Castro, Pedro Henrique
AU - Bladi, Maha Al
AU - Cox, Laura M.
AU - Hodgetts, Kevin J.
AU - Hahn, Mark E.
AU - Mildner, Alexander
AU - Korzenik, Joshua
AU - Hauser, Russ
AU - Snapper, Scott B.
AU - Quintana, Francisco J.
N1 - Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2022/11/24
Y1 - 2022/11/24
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85140208400&partnerID=8YFLogxK
U2 - 10.1038/s41586-022-05308-6
DO - 10.1038/s41586-022-05308-6
M3 - Article
C2 - 36266581
AN - SCOPUS:85140208400
SN - 0028-0836
VL - 611
SP - 801
EP - 809
JO - Nature
JF - Nature
IS - 7937
ER -