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Cytokine Tuning of Intestinal Epithelial Function

Overview
Journal Front Immunol
Date 2018 Jun 21
PMID 29922293
Citations 147
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Abstract

The intestine serves as both our largest single barrier to the external environment and the host of more immune cells than any other location in our bodies. Separating these potential combatants is a single layer of dynamic epithelium composed of heterogeneous epithelial subtypes, each uniquely adapted to carry out a subset of the intestine's diverse functions. In addition to its obvious role in digestion, the intestinal epithelium is responsible for a wide array of critical tasks, including maintaining barrier integrity, preventing invasion by microbial commensals and pathogens, and modulating the intestinal immune system. Communication between these epithelial cells and resident immune cells is crucial for maintaining homeostasis and coordinating appropriate responses to disease and can occur through cell-to-cell contact or by the release or recognition of soluble mediators. The objective of this review is to highlight recent literature illuminating how cytokines and chemokines, both those made by and acting on the intestinal epithelium, orchestrate many of the diverse functions of the intestinal epithelium and its interactions with immune cells in health and disease. Areas of focus include cytokine control of intestinal epithelial proliferation, cell death, and barrier permeability. In addition, the modulation of epithelial-derived cytokines and chemokines by factors such as interactions with stromal and immune cells, pathogen and commensal exposure, and diet will be discussed.

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References
1.
Sedger L, McDermott M . TNF and TNF-receptors: From mediators of cell death and inflammation to therapeutic giants - past, present and future. Cytokine Growth Factor Rev. 2014; 25(4):453-72. DOI: 10.1016/j.cytogfr.2014.07.016. View

2.
Gunther C, Buchen B, He G, Hornef M, Torow N, Neumann H . Caspase-8 controls the gut response to microbial challenges by Tnf-α-dependent and independent pathways. Gut. 2014; 64(4):601-10. PMC: 4392221. DOI: 10.1136/gutjnl-2014-307226. View

3.
Howitt M, Lavoie S, Michaud M, Blum A, Tran S, Weinstock J . Tuft cells, taste-chemosensory cells, orchestrate parasite type 2 immunity in the gut. Science. 2016; 351(6279):1329-33. PMC: 5528851. DOI: 10.1126/science.aaf1648. View

4.
Scheibe K, Backert I, Wirtz S, Hueber A, Schett G, Vieth M . IL-36R signalling activates intestinal epithelial cells and fibroblasts and promotes mucosal healing in vivo. Gut. 2016; 66(5):823-838. DOI: 10.1136/gutjnl-2015-310374. View

5.
Maywald R, Doerner S, Pastorelli L, De Salvo C, Benton S, Dawson E . IL-33 activates tumor stroma to promote intestinal polyposis. Proc Natl Acad Sci U S A. 2015; 112(19):E2487-96. PMC: 4434739. DOI: 10.1073/pnas.1422445112. View