Ly49E expression on CD8αα-expressing intestinal intraepithelial lymphocytes plays no detectable role in the development and progression of experimentally induced inflammatory bowel diseases

PLoS One. 2014 Oct 13;9(10):e110015. doi: 10.1371/journal.pone.0110015. eCollection 2014.

Abstract

The Ly49E NK receptor is a unique inhibitory receptor, presenting with a high degree of conservation among mouse strains and expression on both NK cells and intraepithelial-localised T cells. Amongst intraepithelial-localised T cells, the Ly49E receptor is abundantly expressed on CD8αα-expressing innate-like intestinal intraepithelial lymphocytes (iIELs), which contribute to front-line defense at the mucosal barrier. Inflammatory bowel diseases (IBDs), encompassing Crohn's disease and ulcerative colitis, have previously been suggested to have an autoreactive origin and to evolve from a dysbalance between regulatory and effector functions in the intestinal immune system. Here, we made use of Ly49E-deficient mice to characterize the role of Ly49E receptor expression on CD8αα-expressing iIELs in the development and progression of IBD. For this purpose we used the dextran sodium sulphate (DSS)- and trinitrobenzenesulfonic-acid (TNBS)-induced colitis models, and the TNFΔARE ileitis model. We show that Ly49E is expressed on a high proportion of CD8αα-positive iIELs, with higher expression in the colon as compared to the small intestine. However, Ly49E expression on small intestinal and colonic iIELs does not influence the development or progression of inflammatory bowel diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD8 Antigens / metabolism*
  • Cell Count
  • Colitis / metabolism
  • Colitis / pathology
  • Colon / metabolism
  • Colon / pathology
  • Dextran Sulfate
  • Disease Progression*
  • Epithelial Cells / pathology*
  • Ileitis / metabolism
  • Ileitis / pathology
  • Inflammatory Bowel Diseases / chemically induced
  • Inflammatory Bowel Diseases / metabolism
  • Inflammatory Bowel Diseases / pathology*
  • Intestines / pathology*
  • Lymphocytes / pathology*
  • Mice, Inbred C57BL
  • Mice, Knockout
  • NK Cell Lectin-Like Receptor Subfamily A / metabolism*
  • Receptors, Natural Killer Cell / metabolism
  • Trinitrobenzenesulfonic Acid
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • CD8 Antigens
  • CD8 antigen, alpha chain
  • NK Cell Lectin-Like Receptor Subfamily A
  • Receptors, Natural Killer Cell
  • Tumor Necrosis Factor-alpha
  • Trinitrobenzenesulfonic Acid
  • Dextran Sulfate

Grants and funding

This work was supported by grants from the Foundation against Cancer, a foundation of public interest (2010-166) (http://www.kanker.be/grants) (G.L.), by the Fund for Scientific Research (FWO) (G.0187.13) (http://www.fwo.be/en/fellowships-funding/research-projects/research-project/) (G.L.) and by the BOF of Ghent University (BOF11/GOA/005) (http://www.ugent.be/nl/onderzoek/financiering/bof/goa/overzicht.htm) (J.P, G.L., B.V, T.T.). A.V.A, J.F., M.V. are supported by the Institute for the Promotion of Innovation through Science and Technology Flanders (IWT-Vlaanderen) (http://www.iwt.be/subsidies/sb). S.T. is supported by the BOF of Ghent University. T.K. is supported by the FWO. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.