IL-1 beta and IFN-gamma induce the regenerative epidermal phenotype of psoriasis in the transwell skin organ culture system. IFN-gamma up-regulates the expression of keratin 17 and keratinocyte transglutaminase via endogenous IL-1 production

J Pathol. 1999 Feb;187(3):358-64. doi: 10.1002/(SICI)1096-9896(199902)187:3<358::AID-PATH253>3.0.CO;2-8.

Abstract

Skin biopsies from healthy human skin and non-lesional skin from patients with psoriasis were cultured for 24 h and stimulated with interleukin-1 beta (IL-1 beta) and interferon-gamma (IFN-gamma) in a skin organ culture model and the induction of the psoriasiform regenerative epidermal phenotype was analysed using immunostaining. In the presence of IL-1 beta, the psoriasiform regenerative epidermal phenotype was clearly induced. This involved strong up-regulation of the expression of keratin 16, keratin 17, and keratinocyte transglutaminase (TGk) in the suprabasal layers, strong up-regulation and a shift of the expression of keratin 5 and integrin beta 1 from the basal to suprabasal keratinocytes, and induction of the expression of ICAM-1 and HLA-DR on basal keratinocytes. The effects of IL-1 beta in the organ cultures of normal skin could be completely neutralized by anti-IL-1 polyclonal antibodies. The effects of IFN-gamma in healthy and non-lesional psoriatic skin were qualitatively similar to those of IL-1 beta. The IFN-gamma-induced epidermal expression of keratin 17 and TGk could be completely blocked by culturing the biopsies in the presence of IL-1ra or anti-IL-1 antibodies, while the induction of HLA-DR and ICAM-1 was not inhibited. The induction of the psoriasiform regenerative epidermal phenotype by IFN-gamma is partially mediated via endogenous epidermal IL-1.

MeSH terms

  • Adult
  • Aged
  • Epidermis / metabolism
  • Female
  • Humans
  • Immunoenzyme Techniques
  • Interferon-gamma / pharmacology*
  • Interleukin-1 / biosynthesis
  • Interleukin-1 / pharmacology*
  • Keratinocytes / enzymology
  • Keratins / metabolism*
  • Male
  • Middle Aged
  • Organ Culture Techniques
  • Psoriasis / immunology*
  • Psoriasis / metabolism
  • Recombinant Proteins / pharmacology
  • Skin / immunology
  • Transglutaminases / metabolism*
  • Up-Regulation

Substances

  • Interleukin-1
  • Recombinant Proteins
  • Keratins
  • Interferon-gamma
  • Transglutaminases