Alveolar macrophage apoptosis contributes to pneumococcal clearance in a resolving model of pulmonary infection

J Immunol. 2003 Nov 15;171(10):5380-8. doi: 10.4049/jimmunol.171.10.5380.

Abstract

The role of alveolar macrophages (AM) in host defense against pulmonary infection has been difficult to establish using in vivo models. This may reflect a reliance on models of fulminant infection. To establish a unique model of resolving infection, with which to address the function of AM, C57BL/6 mice received low-dose intratracheal administration of pneumococci. Administration of low doses of pneumococci produced a resolving model of pulmonary infection characterized by clearance of bacteria without features of pneumonia. AM depletion in this model significantly increased bacterial outgrowth in the lung. Interestingly, a significant increase in the number of apoptotic AM was noted with the low-dose infection as compared with mock infection. Caspase inhibition in this model decreased AM apoptosis and increased the number of bacteremic mice, indicating a novel role for caspase activation in pulmonary innate defense against pneumococci. These results suggest that AM play a key role in clearance of bacteria from the lung during subclinical infection and that induction of AM apoptosis contributes to the microbiologic host defense against pneumococci.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Chloromethyl Ketones / administration & dosage
  • Animals
  • Apoptosis / immunology*
  • Bacteremia / enzymology
  • Bacteremia / immunology
  • Bacteremia / microbiology
  • Caspase Inhibitors
  • Cell Count
  • Cysteine Proteinase Inhibitors / administration & dosage
  • Disease Models, Animal*
  • Dose-Response Relationship, Immunologic
  • Female
  • Immunity, Innate
  • Injections, Intraperitoneal
  • Intubation, Intratracheal
  • Macrophages, Alveolar / enzymology
  • Macrophages, Alveolar / immunology*
  • Macrophages, Alveolar / microbiology*
  • Macrophages, Alveolar / pathology
  • Mice
  • Mice, Inbred C57BL
  • Pneumonia, Pneumococcal / enzymology
  • Pneumonia, Pneumococcal / immunology*
  • Pneumonia, Pneumococcal / microbiology*
  • Pneumonia, Pneumococcal / pathology
  • Streptococcus pneumoniae / growth & development
  • Streptococcus pneumoniae / immunology
  • Up-Regulation / immunology

Substances

  • Amino Acid Chloromethyl Ketones
  • Caspase Inhibitors
  • Cysteine Proteinase Inhibitors
  • benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone