Gamma delta intraepithelial lymphocytes drive tumor necrosis factor-alpha responsiveness to intestinal iron challenge: relevance to hemochromatosis

Immunol Rev. 1999 Feb:167:223-32. doi: 10.1111/j.1600-065x.1999.tb01395.x.

Abstract

The dependence of intestinal epithelial cell (IEC) growth and differentiation on intraepithelial lymphocytes (IELs) expressing the gamma/delta (gamma delta) T-cell receptor (TCR), suggested a potential role for gamma delta + IELs in the regulation of iron absorption. We therefore examined the levels of hepatic iron and the IEL cytokine responses in C57BL/6J control and class I and TCR knockout lines (placed on a C57BL/6J genetic background) following the administration of supplemental dietary iron. The highest level of liver iron was found in the beta 2-microglobulin knockout (beta 2m-/-) mice followed by the TCR-delta knockout (TCR delta-/-) animals. TCR-alpha knockout (TCR alpha-/-) and control animals did not differ in their iron levels. Liver iron loading correlated inversely with the ability of the mice to generate an IEL tumor necrosis factor (TNF)-alpha response. These observations suggest a model in which IEC iron loading is communicated to IELs via the HFE class I protein. The result of this communication is the initiation of TNF-alpha release by gamma delta + IELs (sustained by macrophages and dendritic cells) contributing to the upregulation of ferritin expression and possibly to the normal maintenance of the IEC apoptotic pathway.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cytokines / metabolism
  • HLA Antigens / biosynthesis
  • HLA Antigens / physiology
  • Hemochromatosis / immunology*
  • Hemochromatosis / metabolism*
  • Hemochromatosis / pathology
  • Hemochromatosis Protein
  • Histocompatibility Antigens Class I / biosynthesis
  • Histocompatibility Antigens Class I / physiology
  • Humans
  • Intestinal Absorption / immunology
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / metabolism*
  • Intestinal Mucosa / pathology
  • Iron / pharmacokinetics*
  • Liver / metabolism
  • Lymphocytes / metabolism*
  • Membrane Proteins*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Models, Biological
  • Molecular Sequence Data
  • Receptors, Antigen, T-Cell, gamma-delta / physiology*
  • Spleen / metabolism
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Cytokines
  • HFE protein, human
  • HLA Antigens
  • Hemochromatosis Protein
  • Hfe protein, mouse
  • Histocompatibility Antigens Class I
  • Membrane Proteins
  • Receptors, Antigen, T-Cell, gamma-delta
  • Tumor Necrosis Factor-alpha
  • Iron