Suppression of interleukin 1alpha and interleukin 1beta in human limbal epithelial cells cultured on the amniotic membrane stromal matrix

Br J Ophthalmol. 2001 Apr;85(4):444-9. doi: 10.1136/bjo.85.4.444.

Abstract

Aims: Amniotic membrane (AM) transplantation reduces inflammation in a variety of ocular surface disorders. The aim of this study was to determine if AM stroma suppresses the expression of the IL-1 gene family in cultured human corneal limbal epithelial cells.

Methods: Human corneal limbal epithelial cells were cultured from limbocorneal explants of donor eyes on plastic or on the AM stroma. Transcript expression of IL-1alpha, IL-1beta, IL-1 receptor antagonist (RA), and GAPDH was compared with or without addition of lipopolysaccharide to their serum-free media for 24 hours using RNAse protection assay (RPA). Their protein production in the supernatant was analysed by ELISA.

Results: Expression of IL-1alpha and IL-1beta transcripts and proteins was significantly reduced by cells cultured on the AM stromal matrix compared with plastic cultures whether lipopolysaccharide was added or not. Moreover, expression of IL-1 RA by cells cultured in the lipopolysaccharide-free medium was upregulated by AM stromal matrix. The ratio between IL-1 RA and IL-1alpha protein levels in AM cultures was higher than in plastic cultures.

Conclusions: AM stromal matrix markedly suppresses lipopolysaccharide induced upregulation of both IL-1alpha and IL-1beta. These data may explain in part the effect of AM transplantation in reducing ocular surface inflammation, underscoring the unique feature of the AM as a substrate for tissue engineering.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amnion / physiology*
  • Biological Dressings*
  • Cells, Cultured
  • Enzyme-Linked Immunosorbent Assay
  • Epithelium, Corneal / physiology*
  • Female
  • Gene Expression
  • Glyceraldehyde-3-Phosphate Dehydrogenases / physiology
  • Humans
  • Interleukin-1 / genetics
  • Interleukin-1 / physiology*
  • Limbus Corneae / cytology*
  • Lipopolysaccharides / pharmacology
  • Receptors, Interleukin-1 / antagonists & inhibitors
  • Ribonucleases / physiology
  • Up-Regulation / physiology

Substances

  • Interleukin-1
  • Lipopolysaccharides
  • Receptors, Interleukin-1
  • Glyceraldehyde-3-Phosphate Dehydrogenases
  • Ribonucleases