LPS-induced ROS generation and changes in glutathione level and their relation to the maturation of human monocyte-derived dendritic cells

Life Sci. 2006 Jan 25;78(9):926-33. doi: 10.1016/j.lfs.2005.05.106. Epub 2005 Nov 8.

Abstract

Lipopolysaccharide (LPS)-induced reactive oxygen species (ROS) generation and the concomitant decline in the ratio of reduced glutathione (GSH) to oxidized glutathione (GSSG) were demonstrated in human monocyte-derived dendritic cells (DC). Further, their relation to the maturation of DC, characterized by the production of cytokines, up-regulation of cell surface molecules and allo-stimulatory capacity, was examined. The LPS-induced ROS generation was demonstrated using electron paramagnetic resonance spectroscopy in intact cells, and was also confirmed using laser scanning confocal microscopy. The GSH/GSSG was assesed using a glutathione assay kit. When the DC were treated with alpha-phenyl-tert-butylnitrone, the ROS generation was attenuated, but the declined GSH/GSSG was not attenuated, and only cytokine production was suppressed among the above-mentioned maturation characteristics. When the DC were treated with glutathione monoethyl ester, both the ROS generation and the declined GSH/GSSG were attenuated, and the maturation characteristics were all suppressed. These findings suggest that the LPS-induced ROS generation and the concomitant decline in GSH/GSSG occur in human monocyte-derived DC and that the former is involved in cytokine production, while the latter is involved in the up-regulation of cell surface molecules and allo-stimulatory capacity. Since the cytokine production and the allo-stimulatory capacity of DC play an important role in inflammatory and immune responses, differential regulation of the ROS generation and the declined GSH/GSSG may be useful as therapeutic tools in diseases where both responses become entangled, such as sepsis and graft-versus-host disease.

MeSH terms

  • Antigens, Surface / metabolism
  • Cells, Cultured
  • Cyclic N-Oxides
  • Cytokines / metabolism
  • Dendritic Cells / drug effects
  • Dendritic Cells / enzymology
  • Dendritic Cells / metabolism*
  • Flow Cytometry
  • Glutathione / analogs & derivatives
  • Glutathione / metabolism*
  • Glutathione / pharmacology
  • Humans
  • Immunoblotting
  • Indicators and Reagents
  • Interleukin-12 / biosynthesis
  • Lipopolysaccharides / pharmacology*
  • Lymphocyte Culture Test, Mixed
  • Microscopy, Confocal
  • Monocytes / drug effects
  • Monocytes / enzymology
  • Monocytes / metabolism*
  • Nitric Oxide Synthase Type II / biosynthesis
  • Nitrogen Oxides / pharmacology
  • Reactive Oxygen Species / metabolism*
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Up-Regulation / physiology

Substances

  • Antigens, Surface
  • Cyclic N-Oxides
  • Cytokines
  • Indicators and Reagents
  • Lipopolysaccharides
  • Nitrogen Oxides
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • Interleukin-12
  • phenyl-N-tert-butylnitrone
  • S-ethyl glutathione
  • Nitric Oxide Synthase Type II
  • Glutathione