Cell host & microbe · 2021
Western diet induces Paneth cell defects through microbiome alterations and farnesoid X receptor and type I interferon activation.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Liu Ta-Chiang, Kern Justin T, Jain Umang, Sonnek Naomi M, Xiong Shanshan, Simpson Katherine F, VanDussen Kelli L, Winkler Emma S, Haritunians Talin, Malique Atika, Lu Qiuhe, Sasaki Yo, Storer Chad, Diamond Michael S, Head Richard D, McGovern Dermot P B, Stappenbeck Thaddeus S
Аннотация
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.
Предметные рубрики MeSH
AnimalsBile Acids and SaltsCells, CulturedDiet, High-FatDiet, WesternDisease Models, AnimalGastrointestinal MicrobiomeGene Expression ProfilingHumansImmunity, InnateInterferon Type IIntestinal MucosaMiceMice, Inbred C57BLObesityPaneth CellsReceptors, Cytoplasmic and NuclearSignal TransductionReceptor, Farnesoid X-Activated