SNAP-23 regulates phagosome formation and maturation in macrophages

Mol Biol Cell. 2012 Dec;23(24):4849-63. doi: 10.1091/mbc.E12-01-0069. Epub 2012 Oct 19.

Abstract

Synaptosomal associated protein of 23 kDa (SNAP-23), a plasma membrane-localized soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE), has been implicated in phagocytosis by macrophages. For elucidation of its precise role in this process, a macrophage line overexpressing monomeric Venus-tagged SNAP-23 was established. These cells showed enhanced Fc receptor-mediated phagocytosis. Detailed analyses of each process of phagocytosis revealed a marked increase in the production of reactive oxygen species within phagosomes. Also, enhanced accumulation of a lysotropic dye, as well as augmented quenching of a pH-sensitive fluorophore were observed. Analyses of isolated phagosomes indicated the critical role of SNAP-23 in the functional recruitment of the NADPH oxidase complex and vacuolar-type H(+)-ATPase to phagosomes. The data from the overexpression experiments were confirmed by SNAP-23 knockdown, which demonstrated a significant delay in phagosome maturation and a reduction in uptake activity. Finally, for analyzing whether phagosomal SNAP-23 entails a structural change in the protein, an intramolecular Förster resonance energy transfer (FRET) probe was constructed, in which the distance within a TagGFP2-TagRFP was altered upon close approximation of the N-termini of its two SNARE motifs. FRET efficiency on phagosomes was markedly enhanced only when VAMP7, a lysosomal SNARE, was coexpressed. Taken together, our results strongly suggest the involvement of SNAP-23 in both phagosome formation and maturation in macrophages, presumably by mediating SNARE-based membrane traffic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Line
  • Fluorescence Resonance Energy Transfer
  • Humans
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Lysosomes / metabolism
  • Macrophages / cytology
  • Macrophages / metabolism*
  • Mice
  • Microscopy, Confocal
  • NADPH Oxidases / metabolism
  • Phagocytosis
  • Phagosomes / metabolism*
  • Protein Binding
  • Qa-SNARE Proteins / metabolism
  • Qb-SNARE Proteins / genetics
  • Qb-SNARE Proteins / metabolism*
  • Qc-SNARE Proteins / genetics
  • Qc-SNARE Proteins / metabolism*
  • R-SNARE Proteins / metabolism
  • RNA Interference
  • Reactive Oxygen Species / metabolism
  • Vacuolar Proton-Translocating ATPases / metabolism

Substances

  • Luminescent Proteins
  • Qa-SNARE Proteins
  • Qb-SNARE Proteins
  • Qc-SNARE Proteins
  • R-SNARE Proteins
  • Reactive Oxygen Species
  • SNAP23 protein, human
  • NADPH Oxidases
  • Vacuolar Proton-Translocating ATPases