Cell stress-regulated human major histocompatibility complex class I gene expressed in gastrointestinal epithelium.

Veronika Groh(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), Seiamak Bahram(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), Stefan Bauer(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), Andrzej Przemysław Herman(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), M Beauchamp(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), Thomas A. Spies(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa)
Proceedings of the National Academy of Sciences
October 29, 1996
Cited by 1,013Open Access

Abstract

Conventional major histocompatibility complex (MHC) class I genes encode molecules that present intracellular peptide antigens to T cells. They are ubiquitously expressed and regulated by interferon gamma. Two highly divergent human MHC class I genes, MICA and MICB, are regulated by promoter heat shock elements similar to those of HSP70 genes. MICA encodes a cell surface glycoprotein, which is not associated with beta 2-microglobulin, is conformationally stable independent of conventional class I peptide ligands, and almost exclusively expressed in gastrointestinal epithelium. Thus, this MHC class I molecule may function as an indicator of cell stress and may be recognized by a subset of gut mucosal T cells in an unusual interaction.


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