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March 13, 1998Science1,148 citations

Recognition of Stress-Induced MHC Molecules by Intestinal Epithelial γδ T Cells

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VGVeronika GrohASAlexander SteinleSBStefan Bauer

Key Points

  • To determine how intestinal epithelial Vdelta1 gamma-delta T cells recognize the stress-induced MHC class I-related molecules MICA and MICB.
  • Assessed the recognition of MICA and MICB by human intestinal epithelial T cells expressing diverse Vdelta1 gamma-delta T cell receptors (TCRs).
  • Investigated the structural involvement of alpha1alpha2 domains and evaluated the requirement for antigen processing pathways.
  • Tested stress-induced expression and recognition of MICA and MICB in human intestinal epithelial cell lines.
  • Intestinal epithelial T cells bearing diverse Vdelta1 gamma-delta TCRs recognized both MICA and MICB.
  • Receptor interactions depended on the alpha1alpha2 domains of MICA and MICB and functioned independently of classical antigen processing.
  • Cellular stress induced the expression and immune recognition of MICA and MICB in intestinal epithelial cell models.

Abstract

T cells with variable region Vdelta1 gammadelta T cell receptors (TCRs) are distributed throughout the human intestinal epithelium and may function as sentinels that respond to self antigens. The expression of a major histocompatibility complex (MHC) class I-related molecule, MICA, matches this localization. MICA and the closely related MICB were recognized by intestinal epithelial T cells expressing diverse Vdelta1 gammadelta TCRs. These interactions involved the alpha1alpha2 domains of MICA and MICB but were independent of antigen processing. With intestinal epithelial cell lines, the expression and recognition of MICA and MICB could be stress-induced. Thus, these molecules may broadly regulate protective responses by the Vdelta1 gammadelta T cells in the epithelium of the intestinal tract.

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Cite This Study

Groh et al. (1998) studied this question.

synapsesocial.com/papers/6a12fc9bb761793c20c0eb52https://doi.org/10.1126/science.279.5357.1737
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