Fas ligand released by activated monocytes causes apoptosis of lung epithelial cells in human acute lung injury model in vitro

Biol Pharm Bull. 2008 Mar;31(3):386-90. doi: 10.1248/bpb.31.386.

Abstract

Alveolar epithelial cell death plays a crucial role in the progression of acute lung injury. We have demonstrated up-regulation of Fas expression on alveolar epithelial cells, and soluble Fas ligand secretion from inflammatory cells upon acute lung injury. Here we show that the lipopolysaccharide-stimulated human monocyte cell line THP-1 releases Fas ligand, and that conditioned medium from lipopolysaccharide-stimulated THP-1 cells induces apoptosis of the human pulmonary adenocarcinoma cell line A549. Activation of caspase-3 and -8 is associated with the apoptosis. Gene targeting on Fas in A549 cells by specific small interfering RNA impairs apoptosis induced by conditioned medium from activated THP-1, while that on Fas ligand in THP-1 cells impairs the apoptosis-inducing activity of the conditioned medium produced by lipopolysaccharide-stimulated cells. These results suggest that Fas ligand released by monocytes causes alveolar epithelial cell death through a Fas-dependent apoptotic mechanism in the development of acute lung injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Apoptosis / drug effects*
  • Apoptosis / genetics
  • Cell Line, Tumor
  • Culture Media, Conditioned
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology*
  • Fas Ligand Protein / genetics
  • Fas Ligand Protein / metabolism*
  • Fas Ligand Protein / physiology
  • Humans
  • Lipopolysaccharides / pharmacology
  • Lung / cytology
  • Lung / drug effects
  • Lung / pathology*
  • Lung Diseases* / etiology
  • Lung Diseases* / metabolism
  • Lung Diseases* / pathology
  • Monocytes / cytology
  • Monocytes / drug effects
  • Monocytes / metabolism*
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Transfection
  • fas Receptor / biosynthesis
  • fas Receptor / genetics

Substances

  • Culture Media, Conditioned
  • FAS protein, human
  • Fas Ligand Protein
  • Lipopolysaccharides
  • RNA, Small Interfering
  • fas Receptor