Expression of surfactant protein D in human corneal epithelial cells is upregulated by Pseudomonas aeruginosa

FEMS Immunol Med Microbiol. 2008 Nov;54(2):177-84. doi: 10.1111/j.1574-695X.2008.00461.x. Epub 2008 Jul 22.

Abstract

We reported previously that surfactant protein D (SP-D) was present in human tears and corneal epithelial cells, and that it contributed to tear fluid protection of those cells against Pseudomonas aeruginosa invasion. This suggested a role in ocular innate immunity. Here, we explored the effects of bacterial challenge on SP-D expression by human corneal epithelial cells. Results showed that these cells produced and secreted SP-D constitutively in culture, and that production (mRNA, protein) and secretion of SP-D were upregulated after exposure to heat-killed P. aeruginosa or to purified flagellin or lipopolysaccharide. To begin exploring the mechanism for flagellin-mediated SP-D induction, cells were exposed to purified flagellin or flagellin mutated in the TLR-5-binding domain (L94A, L88A) which reduces IL-8 secretion by A549 respiratory cells. Mutated flagellin did not upregulate IL-8 expression in corneal epithelial cells, but did induce SP-D responses. Mitogen-activated protein kinase inhibitors, especially the JNK inhibitor SP600125, reduced secretion of SP-D, but not production, in the presence of P. aeruginosa. These data show that while SP-D and IL-8 corneal responses are each induced by P. aeruginosa or its antigens, they can involve different regions of the same ligand. The data suggest that separate mechanisms may regulate SP-D secretion and production by human corneal epithelia.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Analysis of Variance
  • Antigens, Bacterial / genetics
  • Antigens, Bacterial / metabolism
  • Cell Line, Transformed
  • Enzyme Inhibitors / pharmacology
  • Epithelium, Corneal / immunology*
  • Epithelium, Corneal / metabolism*
  • Epithelium, Corneal / microbiology
  • Flagellin / genetics
  • Flagellin / immunology
  • Gene Expression Regulation
  • Humans
  • Interleukin-8 / metabolism
  • Ligands
  • Lipopolysaccharides / immunology
  • Point Mutation
  • Pseudomonas aeruginosa / genetics
  • Pseudomonas aeruginosa / immunology*
  • Pulmonary Surfactant-Associated Protein D / genetics
  • Pulmonary Surfactant-Associated Protein D / metabolism*
  • Up-Regulation

Substances

  • Antigens, Bacterial
  • Enzyme Inhibitors
  • Interleukin-8
  • Ligands
  • Lipopolysaccharides
  • Pulmonary Surfactant-Associated Protein D
  • Flagellin