Abstract
Nascent phagosomes, which are derived from the plasma membrane, acquire microbicidal properties through multiple fusion and fission events collectively known as maturation. Here we show that remodeling of the phagosomal membrane is apparent even before sealing, particularly when large particles are ingested. Fluorescent probes targeted to the plasma membrane are cleared from the region lining the particle before engulfment is completed. Extensive clearance was noted for components of the inner as well as outer monolayer of the plasmalemma. Segregation of lipid microdomains was ruled out as the mechanism underlying membrane remodeling, because markers residing in rafts and those that are excluded were similarly depleted. Selective endocytosis was also ruled out. Instead, several lines of evidence indicate that endomembranes inserted by exocytosis at sites of ingestion displace the original membrane constituents from the base of the phagosomal cup. The Fcgamma receptors that trigger phagocytosis remain associated with their ligands. By contrast, Src-family kinases that are the immediate effectors of receptor activation are flushed away from the cup by the incoming membranes. Together with the depletion of phosphoinositides required for signal transduction, the disengagement of receptors from their effectors by bulk membrane remodeling provides a novel means to terminate receptor signaling.
MeSH Terms
Animals
Antigens, CD/metabolism
Bacterial Proteins/metabolism
Biomarkers
Cell Membrane/metabolism,ultrastructure
Endocytosis
Exocytosis
Glycosylphosphatidylinositols/metabolism
Humans
Lipid Metabolism
Luminescent Proteins/metabolism
Macrophages/metabolism,ultrastructure
Membrane Microdomains/metabolism
Mice
Models, Biological
Phagocytosis
Receptors, IgG/metabolism
Chemicals
Antigens, CD
Bacterial Proteins
Biomarkers
Fc gamma receptor IIA
Glycosylphosphatidylinositols
Luminescent Proteins
Receptors, IgG
yellow fluorescent protein, Bacteria
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lee Warren L
Programme in Cell Biology, Hospital for Sick Children,Toronto, Ontario, M5G 1X8 Canada.
Mason David
Schreiber Alan D
Grinstein Sergio
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