SLAT is recruited to the phagosome in FcγR-stimulated
macrophages. A, bone marrow-derived macrophages from wild-type
mice were stimulated with human IgG-coated latex beads. The cells were fixed,
permeabilized, and stained with antibodies to SLAT or GAPDH as indicated; NRS
and normal rabbit IgG (NRIg) were used as negative controls. All
cells were stained with phalloidin to detect F-actin. Representative optical
slice from a confocal micrograph of BMM after 3 min of ingestion of human
IgG-coated latex beads, stained with the indicated antibodies and with
phalloidin. B, representative four serial optical slices from a
confocal micrograph showing recruitment of SLAT on the phagosome along with
F-actin indicated with arrows. C, mean fluorescence
intensity of SLAT and F-actin stain around 15 phagosomes. Data represent
average from three independent experiments.