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Expression of genes for B7-H3 and other T cell ligands by nasal epithelial cells during differentiation and activation

¹Department of Environmental Health Sciences, The Johns Hopkins Bloomberg School of Public Health; and Departments of ²Otolaryngology - Head and Neck Surgery and ³Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205

Submitted 1 May 2003 ; accepted in final form 16 March 2004

Epithelial cells of the human respiratory tract express human leukocyte antigen (HLA) and the costimulatory molecules B7-1 and B7-2. Little is known, however, about the constitutive expression of genes encoding for the more recently identified members of the B7 homolog family of costimulatory molecules or about the influence of cellular differentiation and cytokines on their activity or on that of HLA or B7-1 and B7-2. Human nasal epithelial (HNE) cells were grown at the air-liquid interface (ALI) for 2 or 21 days to model in vivo conditions. Expression of genes for HLA-B and HLA-DR1 increased during mucociliary differentiation during this period and became more similar to HNE cells obtained fresh by brush biopsy from nasal turbinates. Gene transcripts for B7-H3 and B7-H2 were abundantly expressed in cells cultured at the ALI, but neither their activities nor that of B7-2 was significantly altered during differentiation. IFN- and TNF- upregulated mRNA encoding for both HLA molecules, but not for the B7 molecules. This study describes, for the first time, the expression of B7-H3 and B7-H2 by HNE cells and thus expands the range of potential costimulatory signals through which these cells may interact with activated mucosal T lymphocytes. In addition, the results suggest that the extent of mucociliary differentiation of cultured cells may influence this capability.

primary cell culture; human; air-liquid interface; interferon-; tumor necrosis factor-

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