Expression of interleukin-6 in the cornea in response to infection with different strains of Pseudomonas aeruginosa

被引:45
作者
Cole, N
Bao, SS
Willcox, M [1 ]
Husband, AJ
机构
[1] Univ New S Wales, Sch Optometry, CRCERT, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Sch Optometry, CCLRU, Sydney, NSW 2052, Australia
[3] Univ Sydney, Dept Anat & Pathol, Sydney, NSW 2006, Australia
关键词
D O I
10.1128/IAI.67.5.2497-2502.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Strains of Pseudomonas aeruginosa causing keratitis can be either cytotoxic (6206) or invasive (6294), while a strain (Paer1) causing contact lens-induced acute red eye has been shown to be neither. In situ hybridization was used to examine the location and identity of cells expressing interleukin-6 (IL-6) mRNA in the murine cornea and changes in expression in response to infection with different strains of P. aerginosa. The number of IL-6-positive cells was determined by image analysis, IL-6 protein levels were measured by an enzyme-linked immunosorbent assay. BALB/c mice were challenged by use of the wounded-cornea model with P. aeruginosa 6294, 6206, or Paer1 (2 x 10(6) CFU), At time intervals up to 24 h, postchallenge corneal tissue was probed for IL-6 mRNA IL-6 mRNA expression was rapidly elevated in the epithelium in response to strains 6294 and 6206, At the conclusion of the experiments, infiltrating inflammatory cells also stained positively for IL-6 mRNA, In contrast, corneas challenged with strain Paer1 showed significant upregulation of IL-6 mRNA only at 4 h postchallenge. Three distinct patterns of IL-6 mRNA expression in the mouse cornea occur in response to these three ocular isolates of P, aeruginosa, The data obtained for mRNA expression in the cornea for all three strains of P, aeruginosa correlated well with IL-6 protein analysis of whole-eye homogenates. Differences in the cytokine responses to these strains correlate with differences in the pathology associated with each strain and may offer an opportunity to develop strategies for the improved management of ocular inflammation.
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页码:2497 / 2502
页数:6
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