Fig. 3.
Fig. 3. CD34+/CD86+ cells cultured in SCF plus GM-CSF acquire the morphology and phagocytic properties of macrophages. Cytospins were prepared after 9 days of culture in the presence of SCF and GM-CSF, followed by Wright-Giemsa staining and microscopic analysis. CD34+/CD86−precursors gave origin predominantly to granulocytes, in addition to a small number of monocytes and macrophages (A; 100× amplification using oil immersion). CD34+/CD86+precursors generated macrophages (B). In a phagocytosis assay, latex particles were internalized by 12% of CD34+/CD86− cell progeny stimulated by SCF plus GM-CSF (C) compared with 61% of CD34+/CD86+ cell progeny stimulated by SCF plus GM-CSF (D).

CD34+/CD86+ cells cultured in SCF plus GM-CSF acquire the morphology and phagocytic properties of macrophages. Cytospins were prepared after 9 days of culture in the presence of SCF and GM-CSF, followed by Wright-Giemsa staining and microscopic analysis. CD34+/CD86precursors gave origin predominantly to granulocytes, in addition to a small number of monocytes and macrophages (A; 100× amplification using oil immersion). CD34+/CD86+precursors generated macrophages (B). In a phagocytosis assay, latex particles were internalized by 12% of CD34+/CD86 cell progeny stimulated by SCF plus GM-CSF (C) compared with 61% of CD34+/CD86+ cell progeny stimulated by SCF plus GM-CSF (D).

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