Surfactant protein A inhibits alveolar macrophage cytokine production by CD14-independent pathway

Am J Physiol Lung Cell Mol Physiol. 2004 Jan;286(1):L129-36. doi: 10.1152/ajplung.00427.2002. Epub 2003 Sep 5.

Abstract

The lung collectin surfactant protein A (SP-A) has both anti-inflammatory and prophagocytic activities. We and others previously showed that SP-A inhibits the macrophage production of tumor necrosis factor (TNF)-alpha stimulated by the gram-negative bacterial component LPS. We propose that SP-A decreases the production of proinflammatory cytokines by alveolar macrophages via a CD14-independent mechanism. SP-A inhibited LPS-simulated TNF-alpha production in rat and mouse macrophages in the presence and absence of serum (72% and 42% inhibition, respectively). In addition, SP-A inhibited LPS-induced mRNA levels for TNF-alpha, IL-1 alpha, and IL-1 beta as well as NF-kappa B DNA binding activity. SP-A also diminished ultrapure LPS-stimulated TNF-alpha produced by wild-type and CD14-null mouse alveolar macrophages by 58% and 88%, respectively. Additionally, SP-A inhibited TNF-alpha stimulated by PMA in both wild-type and TLR4-mutant macrophages. These data suggest that SP-A inhibits inflammatory cytokine production in a CD14-independent manner and also by mechanisms independent of the LPS signaling pathway.

Publication types

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

MeSH terms

  • Animals
  • Carcinogens / pharmacology
  • Cells, Cultured
  • Lipopolysaccharide Receptors / genetics*
  • Lipopolysaccharides / pharmacology
  • Macrophages, Alveolar / cytology
  • Macrophages, Alveolar / immunology
  • Macrophages, Alveolar / metabolism*
  • Male
  • Mice
  • Mice, Inbred C3H
  • Mice, Mutant Strains
  • NF-kappa B / metabolism
  • Pulmonary Surfactant-Associated Protein A / metabolism
  • Pulmonary Surfactant-Associated Protein A / pharmacology*
  • RNA, Messenger / analysis
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • Specific Pathogen-Free Organisms
  • Tetradecanoylphorbol Acetate / pharmacology
  • Transcription, Genetic / immunology
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Carcinogens
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • NF-kappa B
  • Pulmonary Surfactant-Associated Protein A
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Tetradecanoylphorbol Acetate