Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2011 Jan;343(1):5-12.
doi: 10.1007/s00441-010-1082-5. Epub 2010 Nov 23.

Intestinal epithelial cells and their role in innate mucosal immunity

Affiliations
Review

Intestinal epithelial cells and their role in innate mucosal immunity

A L Maldonado-Contreras et al. Cell Tissue Res. 2011 Jan.

Abstract

The mucosal surfaces of the respiratory, gastrointestinal and urogenital tracts are covered by a layer of epithelial cells that are responsible for sensing and promoting a host immune response in order to establish the limits not only for commensal microorganisms but also for foreign organisms or particles. This is a remarkable task as the human body represents a composite of about 10 trillion human-self cells plus non-self cells from autochthonous or indigenous microbes that outnumber human cells 10:1. Hence, the homeostasis of epithelial cells that line mucosal surfaces relies on a fine-tuned immune system that patrols the boundaries between human and microbial cells. In the case of the intestine, the epithelial layer is composed of at least six epithelial cell lineages that act as a physiological barrier in addition to aiding digestion and the absorption of nutrients, water and electrolytes. In this review, we highlight the immense role of the intestinal epithelium in coordinating the mucosal innate immune response.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Representation of intestinal epithelial cell activities that regulate innate mucosal immunity (AMPs antimicrobial peptides, IILs interleukins, IgA immunoglobulin A, pIgAR polimeric immunoglobulin A receptor, LL-37 human cathelicidin, LPS lipopolysaccharide, M cells microfold cells, Mϕ macrophage, MAPK mitogen-activated protein kinases, MYD88, TRIF, TIRAP, TRAM, Rip2 adaptor proteins, NFB nuclear factor kappa-B, NOD Nucleotide-binding oligomerization domain, PAMP’s pathogen-associated molecular patterns, TLR Toll-like receptors)

Similar articles

Cited by

References

    1. Abreu MT, Vora P, Faure E, Thomas LS, Arnold ET, Arditi M. Decreased expression of Toll-like receptor-4 and MD-2 correlates with intestinal epithelial cell protection against dysregulated proinflammatory gene expression in response to bacterial lipopolysaccharide. J Immunol. 2001;167:1609–1616. - PubMed
    1. Ando-Akatsuka Y, Saitou M, Hirase T, Kishi M, Sakakibara A, Itoh M, Yonemura S, Furuse M, Tsukita S. Interspecies diversity of the occludin sequence: cDNA cloning of human, mouse, dog, and rat-kangaroo homologues. J Cell Biol. 1996;133:43–47. - PMC - PubMed
    1. Apodaca G, Bomsel M, Arden J, Breitfeld PP, Tang K, Mostov KE. The polymeric immunoglobulin receptor. A model protein to study transcytosis. J Clin Invest. 1991;87:1877–1882. - PMC - PubMed
    1. Arijs I, De Hertogh G, Lemaire K, Quintens R, Van Lommel L, Van Steen K, Leemans P, Cleynen I, Van Assche G, Vermeire S, Geboes K, Schuit F, Rutgeerts P. Mucosal gene expression of antimicrobial peptides in inflammatory bowel disease before and after first infliximab treatment. PLoS ONE. 2009;4:e7984. - PMC - PubMed
    1. Barnich N, Aguirre JE, Reinecker HC, Xavier R, Podolsky DK. Membrane recruitment of NOD2 in intestinal epithelial cells is essential for nuclear factor-{kappa}B activation in muramyl dipeptide recognition. J Cell Biol. 2005;170:21–26. - PMC - PubMed

LinkOut - more resources