Author
Listed:
- Liliana M. Sanmarco
(Brigham and Women’s Hospital, Harvard Medical School)
- Chun-Cheih Chao
(Brigham and Women’s Hospital, Harvard Medical School)
- Yu-Chao Wang
(National Yang Ming Chiao Tung University)
- Jessica E. Kenison
(Brigham and Women’s Hospital, Harvard Medical School)
- Zhaorong Li
(Brigham and Women’s Hospital, Harvard Medical School)
- Joseph M. Rone
(Brigham and Women’s Hospital, Harvard Medical School)
- Claudia M. Rejano-Gordillo
(Brigham and Women’s Hospital, Harvard Medical School)
- Carolina M. Polonio
(Brigham and Women’s Hospital, Harvard Medical School)
- Cristina Gutierrez-Vazquez
(Brigham and Women’s Hospital, Harvard Medical School)
- Gavin Piester
(Brigham and Women’s Hospital, Harvard Medical School
University of Rochester Medical Center)
- Agustin Plasencia
(Brigham and Women’s Hospital, Harvard Medical School)
- Lucinda Li
(Brigham and Women’s Hospital, Harvard Medical School)
- Federico Giovannoni
(Brigham and Women’s Hospital, Harvard Medical School)
- Hong-Gyun Lee
(Brigham and Women’s Hospital, Harvard Medical School)
- Camilo Faust Akl
(Brigham and Women’s Hospital, Harvard Medical School)
- Michael A. Wheeler
(Brigham and Women’s Hospital, Harvard Medical School
The Broad Institute of Harvard and MIT)
- Ivan Mascanfroni
(Brigham and Women’s Hospital, Harvard Medical School)
- Merja Jaronen
(Brigham and Women’s Hospital, Harvard Medical School)
- Moneera Alsuwailm
(Brigham and Women’s Hospital, Harvard Medical School)
- Patrick Hewson
(Brigham and Women’s Hospital, Harvard Medical School)
- Ada Yeste
(Brigham and Women’s Hospital, Harvard Medical School)
- Brian M. Andersen
(Brigham and Women’s Hospital, Harvard Medical School
Dana-Farber Cancer Institute, Harvard Medical School)
- Diana G. Franks
(Woods Hole Oceanographic Institution)
- Chien-Jung Huang
(National Yang Ming Chiao Tung University)
- Millicent Ekwudo
(Brigham and Women’s Hospital, Harvard Medical School)
- Emily C. Tjon
(Brigham and Women’s Hospital, Harvard Medical School)
- Veit Rothhammer
(Brigham and Women’s Hospital, Harvard Medical School)
- Maisa Takenaka
(Brigham and Women’s Hospital, Harvard Medical School)
- Kalil Alves Lima
(Brigham and Women’s Hospital, Harvard Medical School)
- Mathias Linnerbauer
(Brigham and Women’s Hospital, Harvard Medical School)
- Lydia Guo
(Brigham and Women’s Hospital, Harvard Medical School)
- Ruxandra Covacu
(Brigham and Women’s Hospital, Harvard Medical School)
- Hugo Queva
(Brigham and Women’s Hospital, Harvard Medical School)
- Pedro Henrique Fonseca-Castro
(Brigham and Women’s Hospital, Harvard Medical School)
- Maha Al Bladi
(Brigham and Women’s Hospital, Harvard Medical School)
- Laura M. Cox
(Brigham and Women’s Hospital, Harvard Medical School)
- Kevin J. Hodgetts
(Brigham and Women’s Hospital, Harvard Medical School)
- Mark E. Hahn
(Woods Hole Oceanographic Institution)
- Alexander Mildner
(Max-Delbrück-Center for Molecular Medicine (MDC))
- Joshua Korzenik
(Brigham and Women’s Hospital, Harvard Medical School)
- Russ Hauser
(Harvard T. H. Chan School of Public Health)
- Scott B. Snapper
(Boston Children’s Hospital
Harvard Medical School)
- Francisco J. Quintana
(Brigham and Women’s Hospital, Harvard Medical School
The Broad Institute of Harvard and MIT)
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.
Suggested Citation
Liliana M. Sanmarco & Chun-Cheih Chao & Yu-Chao Wang & Jessica E. Kenison & Zhaorong Li & Joseph M. Rone & Claudia M. Rejano-Gordillo & Carolina M. Polonio & Cristina Gutierrez-Vazquez & Gavin Piester, 2022.
"Identification of environmental factors that promote intestinal inflammation,"
Nature, Nature, vol. 611(7937), pages 801-809, November.
Handle:
RePEc:nat:nature:v:611:y:2022:i:7937:d:10.1038_s41586-022-05308-6
DOI: 10.1038/s41586-022-05308-6
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