Heightened expression of MICA enhances the cytotoxicity of NK cells or CD8(+)T cells to human corneal epithelium in vitro

BACKGROUND: Major-histocompatibility-complex class I-related chain A (MICA) antigens are the ligands of NKG2D, which is an activating or coactivating receptor expressed on human NK cells and CD8(+)T cells. We sought to determine whether MICA expression in human corneal epithelium (HCE) could affect the cytotoxicity mediated by NK cells or CD8(+)T cells. METHODS: Cell cultures of HCE were harvested from human donor eyes. Flow cytometric analysis and ELISA was performed to determine the levels of MICA expression on HCE. Then, HCE was transfected with a lentivirus vector expressing MICA and GFP. Flow cytometric analysis, RT-PCR, western blot and ELISA were performed to check the levels of MICA expression. For cytotoxicity testing, allogeneic NK cells and CD8(+)T cells were isolated from peripheral blood mononuclear cells of healthy volunteers by magnetic cell sorting. The cytolytic activity of NK cells and CD8(+)T cells was assessed against MICA-transfected HCE (NK cells: E:T ratio = 3:1; CD8(+)T cells: E:T ratio = 10:1) using the nonradioactive cytotoxicity detection kit lactate deshydrogenase. RESULTS: Surface expression of MICA on corneal epithelium was identified at a low level. A cell line of stable human MICA-transfected corneal epithelium was successfully established. Heightened expression of MICA on HCE was found to promote the cytotoxicity mediated by NK cells or CD8(+)T cells, which could be blocked by an anti-MICA antibody. CONCLUSION: MICA molecules may contribute to cytotoxic responses mediated by activated immune effector cells in corneal epithelium immunity.