The role of IL-1beta in the regulation of IL-8 and IL-6 in human corneal epithelial cells during Pseudomonas aeruginosa colonization

Curr Eye Res. 2001 Dec;23(6):406-14. doi: 10.1076/ceyr.23.6.406.6969.

Abstract

Purpose: Recent studies have shown that the levels of interleukin (IL)-1beta, IL-6 and IL-8 are associated with the severity of infectious diseases. The purpose of this study was to investigate whether IL-1beta regulates the expression of IL-6 and IL-8 in human corneal epithelial cells during Pseudomonas aeruginosa colonization.

Methods: Confluent immortalized human corneal epithelial cells were challenged with P. aeruginosa 6294 in the presence of anti-human IL-1beta antibody or matched control antibody. The cells were also challenged with recombinant IL-1beta protein without bacterial colonization. Expression of IL-1beta, IL-6 and IL-8 mRNA and protein was detected by reverse transcription (RT)-PCR and by enzyme-linked immunosorbent assay (ELISA), respectively. IL-1beta localization was determined by immunohistochemistry.

Results: Human corneal epithelial cells expressed low levels of IL-1beta and high levels of IL-6 and IL-8 during P. aeruginosa colonization. Addition of IL-1beta Ab resulted in a significant decrease (P < 0.05) in IL-8 protein expression at 4 h, 8 h and 12 h. Addition of IL-1beta Ab reduced IL-6 protein expression at 8 h and increased IL-6 protein expression at 12 h. Addition of recombinant IL-1beta protein alone strongly stimulated the expression of IL-8 and IL-6. Immunohistochemical staining showed that IL-1beta protein was present both intracellularly and extracellularly in P. aeruginosa colonized cells.

Conclusions: IL-1beta is able to modulate expression of both IL-6 and IL-8 at transcriptional and post-transcriptional levels in human corneal epithelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Enzyme-Linked Immunosorbent Assay
  • Epithelium, Corneal / metabolism*
  • Epithelium, Corneal / microbiology*
  • Gene Expression Regulation
  • Humans
  • Immunoenzyme Techniques
  • Interleukin-1 / pharmacology
  • Interleukin-1 / physiology*
  • Interleukin-6 / genetics*
  • Interleukin-6 / metabolism
  • Interleukin-8 / genetics*
  • Interleukin-8 / metabolism
  • Pseudomonas aeruginosa / physiology*
  • RNA, Messenger / metabolism
  • Recombinant Proteins / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Interleukin-1
  • Interleukin-6
  • Interleukin-8
  • RNA, Messenger
  • Recombinant Proteins