Surfactant protein-A enhances ureaplasmacidal activity in vitro

Innate Immun. 2011 Apr;17(2):145-51. doi: 10.1177/1753425909360552. Epub 2010 Mar 2.

Abstract

Background: Persistent respiratory tract colonization with Ureaplasma spp. in preterm infants is a significant risk factor for the development of the chronic lung disorder, bronchopulmonary dysplasia (BPD). Surfactant protein-A (SP-A), a lung collectin critical for bacterial clearance and regulating inflammation, is deficient in the preterm lung. In an experimental Ureaplasma-pneumonia model, infected SP-A deficient mice exhibited delayed bacterial clearance and an exaggerated inflammatory response compared to infected wild-type mice. The objective was to analyze the role of SP-A in Ureaplasma clearance in vitro.

Subjects and methods: We analyzed SP-A binding to Ureaplasma isolates and SP-A-mediated ureaplasmal phagocytosis and killing by cultured RAW 264.7 macrophages.

Results: Calcium-dependent SP-A binding was similar among Ureaplasma isolates tested. Pre-incubation of RAW 264.7 cells with SP-A (10-50 μg/ml) enhanced phagocytosis of fluorescein-isothiocyanate (FITC)-labeled Ureaplasma. Surfactant protein-A also increased ureaplasmacidal activity of RAW 264.7 cells by 2.1-fold over 4 h. Pre-incubation of RAW 264.7 cells with 10 μg/ml SP-A reduced lipopolysaccharide (LPS) (100 ng/ml) and Ureaplasma (10(6) color changing units/ml)-stimulated release of tumor necrosis factor-α (TNF-α) by 46% and 43%, respectively, but did not affect transforming growth factor β(1) (TGFβ(1)) release.

Conclusions: These in vitro data confirm that SP-A is important in host defense to perinatally-acquired Ureaplasma infection.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cytotoxicity, Immunologic / drug effects
  • Humans
  • Infant, Newborn
  • Macrophages / drug effects*
  • Macrophages / immunology
  • Macrophages / metabolism
  • Macrophages / microbiology
  • Macrophages / pathology
  • Mice
  • Phagocytosis / drug effects
  • Phagocytosis / immunology
  • Pulmonary Surfactant-Associated Protein A / pharmacology*
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / metabolism*
  • Ureaplasma / immunology*
  • Ureaplasma / pathogenicity
  • Ureaplasma Infections / drug therapy*
  • Ureaplasma Infections / immunology

Substances

  • Pulmonary Surfactant-Associated Protein A
  • Tumor Necrosis Factor-alpha