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Cytokine Tuning of Intestinal Epithelial Function

  1. Author:
    Andrews, Caroline
    McLean, Mairi H.
    Durum, Scott
  2. Author Address

    NCI, Canc & Inflammat Program, Ctr Canc Res, NIH, Frederick, MD 21701 USA.Univ Aberdeen, Sch Med Med Sci & Nutr, Aberdeen, Scotland.
    1. Year: 2018
    2. Date: Jun 5
    3. Epub Date: 2018 06 05
  1. Journal: Frontiers in Immunology
  2. FRONTIERS MEDIA SA,
    1. 9
    2. Pages: 1270
  3. Type of Article: Review
  4. Article Number: 1270
  5. ISSN: 1664-3224
  1. 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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External Sources

  1. DOI: 10.3389/fimmu.2018.01270
  2. PMID: 29922293
  3. PMCID: PMC5996247
  4. WOS: 000434167700001

Library Notes

  1. Fiscal Year: FY2017-2018
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