Involvement of antipain-sensitive protease activity in the interferon-beta-induced UV-refractoriness of Cockayne syndrome fibroblasts

Mutat Res. 1996 Oct 25;357(1-2):177-81. doi: 10.1016/0027-5107(96)00098-x.

Abstract

Fibroblast cells obtained from two siblings and a female patient with Cockayne syndrome (CS), when pretreated with human interferon (HuIFN)-beta prior to irradiation with UV light (254 nm wavelength), exhibited transiently induced fibrinolytic protease activity immediately after the irradiation in association with increased refractoriness to UV cell-killing. A protease inhibitor, antipain, inhibited the induction of protease activity in lysates of the CS fibroblasts from these 3 cases after the combination of HuIFN-beta pretreatment and UV irradiation, whereas elastatinal and 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB) inhibited the activity less than antipain did. Antipain also suppressed the increase in UV-refractoriness of HuIFN-beta-pretreated CS fibroblasts, as revealed by culturing cells for 24 h in medium containing the inhibitor immediately after UV exposure and thereafter evaluating the ability of colony formation by the cells. Thus, an antipain-sensitive protease may be involved in the UV-refractoriness induced by HuIFN-beta in CS fibroblast strains.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antipain / pharmacology
  • Cell Survival / radiation effects
  • Cockayne Syndrome / genetics*
  • Endopeptidases / metabolism
  • Female
  • Humans
  • Interferon-beta / physiology*
  • Male
  • Pedigree
  • Protease Inhibitors / pharmacology
  • Ultraviolet Rays

Substances

  • Protease Inhibitors
  • Antipain
  • Interferon-beta
  • Endopeptidases