| Literature DB >> 31923399 |
Abigail Jarret1, Ruaidhrí Jackson2, Coco Duizer1, Marc E Healy3, Jun Zhao4, Joseph M Rone5, Piotr Bielecki1, Esen Sefik1, Manolis Roulis1, Tyler Rice1, Kisha N Sivanathan5, Ting Zhou1, Angel G Solis1, Hanna Honcharova-Biletska6, Karelia Vélez7, Saskia Hartner8, Jun Siong Low1, Rihao Qu9, Marcel R de Zoete10, Noah W Palm1, Aaron M Ring1, Achim Weber3, Andreas E Moor7, Yuval Kluger11, Roni Nowarski12, Richard A Flavell13.
Abstract
Mucosal barrier immunity is essential for the maintenance of the commensal microflora and combating invasive bacterial infection. Although immune and epithelial cells are thought to be the canonical orchestrators of this complex equilibrium, here, we show that the enteric nervous system (ENS) plays an essential and non-redundant role in governing the antimicrobial protein (AMP) response. Using confocal microscopy and single-molecule fluorescence in situ mRNA hybridization (smFISH) studies, we observed that intestinal neurons produce the pleiotropic cytokine IL-18. Strikingly, deletion of IL-18 from the enteric neurons alone, but not immune or epithelial cells, rendered mice susceptible to invasive Salmonella typhimurium (S.t.) infection. Mechanistically, unbiased RNA sequencing and single-cell sequencing revealed that enteric neuronal IL-18 is specifically required for homeostatic goblet cell AMP production. Together, we show that neuron-derived IL-18 signaling controls tissue-wide intestinal immunity and has profound consequences on the mucosal barrier and invasive bacterial killing.Entities:
Keywords: Salmonella; antimicrobial proteins; barrier immunity; colon; goblet cell; homeostasis; inflammasome; microbiota; mucosal immunology; neuroimmunology
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Year: 2020 PMID: 31923399 PMCID: PMC7339937 DOI: 10.1016/j.cell.2019.12.016
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582