Surfactant protein A enhances Mycobacterium avium ingestion but not killing by rat macrophages

Joseph P Lopez1, Emily Clark, Virginia L Shepherd

  • 1Department of Pathology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

Journal of Leukocyte Biology
|September 10, 2003
PubMed

Insights

Surfactant protein A (SP-A) enhances the uptake of Mycobacterium avium complex (MAC) by macrophages. However, SP-A does not improve the clearance of MAC, unlike other mycobacterial infections.

Area of Science:

  • Pulmonary immunology
  • Innate immune response
  • Macrophage biology

Background:

  • Mycobacterium avium complex (MAC) causes opportunistic infections, particularly in AIDS patients.
  • MAC can enter the respiratory tract and interact with alveolar macrophages and surfactant protein A (SP-A).
  • SP-A is a key component of the lung's innate immunity, previously shown to aid in clearing other mycobacteria.

Purpose of the Study:

  • To investigate the role of SP-A in the clearance of MAC by rat macrophages.
  • To determine if SP-A influences macrophage interaction with MAC.
  • To assess the impact of SP-A on intracellular survival and nitric oxide production during MAC infection.

Main Methods:

  • Cultured rat macrophages were used to study MAC clearance.
  • SP-A opsonization of MAC was performed before macrophage infection.
  • Nitric oxide synthase inhibitors were used to evaluate the NO-dependent pathway.

Main Results:

  • SP-A bound to MAC and enhanced its ingestion by macrophages.
  • SP-A-MAC complexes stimulated the production of nitric oxide (NO) and tumor necrosis factor-alpha.
  • SP-A did not alter the intracellular survival of MAC within macrophages.
  • Inhibitors of inducible NO synthase did not affect MAC clearance, indicating a non-NO-dependent process.

Conclusions:

  • SP-A enhances MAC uptake by alveolar macrophages, similar to its effect on BCG and M. tuberculosis.
  • Unlike other pulmonary pathogens, SP-A does not promote efficient macrophage-mediated clearance of MAC via a nitric oxide-dependent pathway.