Fig. 2.
Fig. 2. Electron microscopy of neutrophils from skin windows after phagocytosis of latex beads. / (A) Cryosection incubated with anti–hCAP-18 and 10-nm protein A-gold. Neutrophil with phagolysosomes (p) containing latex beads. (Inset) Higher magnification of the marked area showing a granule containing hCAP-18 (large arrow) and a phagolysosome also labeled for hCAP-18 (small arrows). Bars, 400 nm; inset, 100 nm. (B) Double-immunogold labeling of hCAP-18 (as a marker of specific granules) with 10-nm gold particles and myeloperoxidase (MPO, as a marker of azurophil granules) with 5-nm gold particles demonstrated that both azurophil and specific granules fused with the phagolysosome. Bar, 100 nm.

Electron microscopy of neutrophils from skin windows after phagocytosis of latex beads.

(A) Cryosection incubated with anti–hCAP-18 and 10-nm protein A-gold. Neutrophil with phagolysosomes (p) containing latex beads. (Inset) Higher magnification of the marked area showing a granule containing hCAP-18 (large arrow) and a phagolysosome also labeled for hCAP-18 (small arrows). Bars, 400 nm; inset, 100 nm. (B) Double-immunogold labeling of hCAP-18 (as a marker of specific granules) with 10-nm gold particles and myeloperoxidase (MPO, as a marker of azurophil granules) with 5-nm gold particles demonstrated that both azurophil and specific granules fused with the phagolysosome. Bar, 100 nm.

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