Cytokine regulation of RANTES production by human retinal pigment epithelial cells

Cell Immunol. 1998 Feb 25;184(1):37-44. doi: 10.1006/cimm.1997.1235.

Abstract

The mechanism whereby inflammatory cells gain access to the retina in posterior intraocular inflammatory disease remains unclear. The chemokine RANTES has the potential to influence the migration of memory T cells and monocytes across the blood-retinal barrier during inflammatory eye disease. We have therefore examined the production of RANTES by cultured human retinal pigment epithelial cells (RPE), which form a part of the blood-retinal barrier, in response to cytokines likely to be present in the microenvironment. IL-1 beta and TNF alpha stimulated RANTES production by these cells. IFN-gamma acted synergistically with TNF alpha to increase RANTES production. In contrast, IL-4 downregulated RANTES production stimulated by TNF alpha. RT-PCR studies showed that RANTES mRNA from RPE followed the same pattern of expression in response to cytokines as did RANTES production indicating that RANTES production was controlled at, or prior to, transcription. RANTES is produced in vitro by RPE in response to the proinflammatory cytokines IL-1 beta, TNF alpha, and IFN-gamma and is therefore likely to play a role in the development of the inflammatory eye disease endogenous posterior uveitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Movement
  • Cells, Cultured
  • Chemokine CCL5 / biosynthesis
  • Chemokine CCL5 / genetics
  • Cytokines / pharmacology*
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Interleukin-1 / pharmacology
  • Interleukin-4 / pharmacology
  • Monocytes / physiology
  • Pigment Epithelium of Eye / cytology
  • Pigment Epithelium of Eye / metabolism*
  • Polymerase Chain Reaction
  • RNA, Messenger / analysis
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Chemokine CCL5
  • Cytokines
  • Interleukin-1
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Interleukin-4