| Literature DB >> 34010595 |
Ta-Chiang Liu1, Justin T Kern2, Umang Jain2, Naomi M Sonnek2, Shanshan Xiong2, Katherine F Simpson2, Kelli L VanDussen2, Emma S Winkler3, Talin Haritunians4, Atika Malique2, Qiuhe Lu2, Yo Sasaki5, Chad Storer5, Michael S Diamond6, Richard D Head5, Dermot P B McGovern4, Thaddeus S Stappenbeck7.
Abstract
Intestinal Paneth cells modulate innate immunity and infection. In Crohn's disease, genetic mutations together with environmental triggers can disable Paneth cell function. Here, we find that a western diet (WD) similarly leads to Paneth cell dysfunction through mechanisms dependent on the microbiome and farnesoid X receptor (FXR) and type I interferon (IFN) signaling. Analysis of multiple human cohorts suggests that obesity is associated with Paneth cell dysfunction. In mouse models, consumption of a WD for as little as 4 weeks led to Paneth cell dysfunction. WD consumption in conjunction with Clostridium spp. increased the secondary bile acid deoxycholic acid levels in the ileum, which in turn inhibited Paneth cell function. The process required excess signaling of both FXR and IFN within intestinal epithelial cells. Our findings provide a mechanistic link between poor diet and inhibition of gut innate immunity and uncover an effect of FXR activation in gut inflammation.Entities:
Keywords: cell-intrinsic; high fat diet; metabolism; microbiota; myeloid cells; obesity; organoids; transcriptomics
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Year: 2021 PMID: 34010595 PMCID: PMC8192497 DOI: 10.1016/j.chom.2021.04.004
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 31.316