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NKG2D ligands are expressed on stressed human airway epithelial cells

¹Department of Environmental Health, Division of Environmental Genetics and Molecular Toxicology, ²Department of Internal Medicine, Pulmonary Division, University of Cincinnati College of Medicine, Cincinnati, Ohio; and ³Amgen Washington, Incorporated, Seattle, Washington

Submitted 25 July 2005 ; accepted in final form 7 February 2006

Immune surveillance of the airways is critical to maintain the integrity and health of the lung. We have identified a family of ligands expressed on the surface of stressed airway epithelial cells whose function is to bind the NKG2D-activating receptor found on several pulmonary lymphocytes, including natural killer cells, ⁺ T cells, and CD8⁺ T cells. We employed real-time PCR and flow cytometry in normal and transformed airway epithelial cell to demonstrate that major histocompatibility complex class I chain-related (MIC) B and the UL-16 binding protein (ULBP) ligands (ULBP1–4) are ubiquitously expressed at the mRNA level in all cell lines. MICA/B surface expression was present on 70% of transformed cell lines but was undetectable on primary cells. We demonstrate that MICA/B and ULBP 1, 2, 3, and 4 expression is rare or absent on the cell surface of unstimulated normal human bronchial epithelial cells although transcripts and intracellular proteins are present. Normal human bronchial epithelial cells exposed to 0.3 mM hydrogen peroxide exhibit an induction of all ligands examined on the cell surface. Surface expression is independent of changes in transcript level or total cellular protein and is mediated by the ERK family of mitogen-activated protein kinases. The induction of NKG2D ligands on stressed airway epithelial cells represents a potentially important mechanism of immune cell activation in regulation of pulmonary health and disease.

MHC class I chain-related molecules A/B; UL-16 binding proteins; natural killer; T cell

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