Mannose-binding lectin (MBL) facilitates opsonophagocytosis of yeasts but not of bacteria despite MBL binding

J Immunol. 2008 Mar 15;180(6):4124-32. doi: 10.4049/jimmunol.180.6.4124.

Abstract

Mannose-binding lectin (MBL) is a serum protein of the innate immune system. After binding to a microorganism, MBL in complex with MBL-associated serine proteases activates the complement system, resulting in cleavage of complement factor C3. Cleaved C3 on the surface of the microorganism mediates opsonization for clearance, but the impact of MBL on subsequent phagocytosis has not been widely studied. We investigated the role of MBL in complement activation and phagocytosis of various bacteria and yeast species by flow cytometry. We measured both the C3 deposition during serum opsonization of fluorescent-labeled microorganisms as well as subsequent uptake of these microorganisms by human neutrophils. In MBL-deficient sera, a consistently decreased C3 deposition on both zymosan and Candida albicans was found and a reduced phagocytosis by neutrophils that was restored by exogenous MBL. This indicates that the lectin pathway of complement activation is important for the opsonophagocytosis of yeasts. In contrast, the C1q-dependent classical pathway dominated in the opsonization and phagocytosis of Staphylococcus aureus, Streptococcus pneumoniae, and Escherichia coli, whereas no effect of MBL was found. Both the lectin and the classical pathway of complement activation were highly amplified by the alternative route for opsonophagocytosis by neutrophils of yeast as well as microbial species. In summary, our data demonstrate that yeast species are preferentially opsonized and subsequently phagocytosed via activation of the lectin pathway of complement, whereas the uptake of bacterial strains was found to be largely MBL independent.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Candida albicans / cytology
  • Candida albicans / immunology
  • Candida albicans / metabolism
  • Complement C3 / metabolism
  • Complement Pathway, Alternative / immunology
  • Escherichia coli / cytology
  • Escherichia coli / immunology
  • Escherichia coli / metabolism
  • Female
  • Humans
  • Male
  • Mannose-Binding Lectin / blood
  • Mannose-Binding Lectin / physiology*
  • Neutrophils / immunology
  • Neutrophils / metabolism
  • Neutrophils / microbiology
  • Opsonin Proteins / blood
  • Opsonin Proteins / physiology*
  • Phagocytosis / immunology*
  • Protein Binding / immunology
  • Saccharomyces cerevisiae / cytology
  • Saccharomyces cerevisiae / immunology
  • Saccharomyces cerevisiae / metabolism
  • Staphylococcus aureus / cytology
  • Staphylococcus aureus / immunology
  • Staphylococcus aureus / metabolism

Substances

  • Complement C3
  • Mannose-Binding Lectin
  • Opsonin Proteins