Protein synthesis-dependent induction of interleukin-1 beta by lipopolysaccharide is inhibited by dexamethasone via mRNA destabilization in human astroglial cells

J Clin Immunol. 1995 Jul;15(4):199-204. doi: 10.1007/BF01541090.

Abstract

Dexamethasone inhibits lipopolysaccharide-induced synthesis of the cytokine, interleukin-1 beta, in cerebrospinal fluid of patients with bacterial meningitis. Along with monocytes, astrocytes are capable of producing lipopolysaccharide-induced interleukin-1 beta in the central nervous system. The objective of this study was to investigate the induction of interleukin-1 beta mRNA by lipopolysaccharide, and the inhibition of this process by dexamethasone, in human astrocytes using the astrocytoma cell line U-373MG as a model system. Dexamethasone-mediated inhibition of induction of interleukin-1 beta mRNA by lipopolysaccharide required a functional glucocorticoid receptor. In contrast to monocytes, lipopolysaccharide induction of interleukin-1 beta mRNA in U-373MG cells required de novo protein synthesis. Dexamethasone also had no effect on lipopolysaccharide-induced interleukin-1 beta transcriptional initiation in U-373MG cells. U-373MG cells were similar to monocytes, however, with respect to the ability of dexamethasone to decrease interleukin-1 beta mRNA half-life. These findings demonstrate that the mode of lipopolysaccharide induction of interleukin-1 beta mRNA, and inhibition of this process by dexamethasone, can vary in different cell types.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Astrocytes / drug effects*
  • Astrocytes / metabolism
  • Astrocytoma / immunology
  • Cycloheximide / pharmacology
  • Dexamethasone / pharmacology*
  • Humans
  • Interleukin-1 / antagonists & inhibitors*
  • Interleukin-1 / biosynthesis
  • Interleukin-1 / genetics*
  • Lipopolysaccharides / pharmacology*
  • Mifepristone / pharmacology
  • Protein Synthesis Inhibitors / pharmacology
  • RNA, Messenger / drug effects*
  • Transcription, Genetic / drug effects
  • Tumor Cells, Cultured

Substances

  • Interleukin-1
  • Lipopolysaccharides
  • Protein Synthesis Inhibitors
  • RNA, Messenger
  • Mifepristone
  • Dexamethasone
  • Cycloheximide