Autologous versus allogeneic T cell-stimulated IL-6 production by dermal fibroblasts

Inflammation. 1997 Aug;21(4):371-8. doi: 10.1023/a:1027310218934.

Abstract

T cells adhere to human dermal fibroblasts (HDF). This cellular interaction leads to a pronounced secretion of the proinflammatory cytokines IL-6 and IL-8 via a juxtacrine stimulation induced by HDF-associated IL-1. Upon stimulation, fibroblasts express various surface proteins such as MCH-I molecules, which may interact with corresponding receptors on T cells. The present study was conducted to further investigate the mechanism of this complex interaction with regard to the secretion of IL-6 in cocultures of T cells and HDF. IL-6 was time- and dose-dependently upregulated in such cocultures. Spatial separation of the cells by microporous membranes resulted in a 90% reduction of IL-6 secretion, but when cells had limited cell contact IL-6 secretion was increased again. Allogeneic cocultures of T cells and HDF showed increased capacity of IL-6 stimulation as compared to autologous cultures. Our results suggest that MHC-I/T cell receptor interaction modulates IL-6 secretion in allogeneic and autologous cocultures.

MeSH terms

  • Cell Communication
  • Cell Separation
  • Coculture Techniques
  • Fibroblasts / metabolism
  • Humans
  • Interleukin-6 / biosynthesis*
  • Skin / cytology
  • Skin / metabolism*
  • T-Lymphocytes / physiology*
  • Time Factors

Substances

  • Interleukin-6