Involvement of interleukin 18 in cataract development in hereditary cataract UPL rats

J Biochem. 2007 Nov;142(5):597-603. doi: 10.1093/jb/mvm168.

Abstract

Our previous studies have demonstrated that lens epithelial damage by excessive nitric oxide causes an elevation in lens opacification in UPL rats, and it has been reported that interferon-gamma production in lens epithelial cells is involved in cataract development. In this study, we investigated the involvement of interleukin (IL)-18, which leads to interferon-gamma, in UPL rat lenses. The opacification of UPL rat lenses starts at 39 days of age. The gene expression levels causing IL-18 activation (IL-18, IL-18 receptor and caspase-1) are increased at 32 days of age, and the expression of mature IL-18 protein in the UPL rat lenses also increases with ageing. On the other hand, the interferon-gamma levels in UPL rat lenses are increased, and the increase in interferon-gamma levels in UPL rat lenses reaches a maximum at 39 days of age. Mature IL-18 expression and interferon-gamma production are achieved prior to the onset of lens opacification. In conclusion, the expression levels of IL-18 in the lenses of UPL rats are increased with aging. In addition, interferon-gamma levels in the lenses of UPL rats are also increased. It is possible that interferon-gamma generated by the activated IL-18 may induce cataract development in UPL rats.

MeSH terms

  • Age Factors
  • Animals
  • Cataract / metabolism*
  • Disease Models, Animal
  • Enzyme-Linked Immunosorbent Assay
  • Eye Diseases, Hereditary / metabolism*
  • Eye Diseases, Hereditary / pathology
  • Interleukin-18 / physiology*
  • Lens, Crystalline / physiology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Interleukin-18