Fig. 6.
Fig. 6. Macrophage development can be restored by PU.1 transduction of PU.1-deficient 503 cells. (A) PU.1 transduction of 503 cells (503-PU) restored the development of cells with typical macrophage appearance as shown by Wright-Giemsa staining. (B) Immuno-cytochemistry was used to show that 503-PU cells expressed the macrophage marker F4/80, unlike the parental cells (503). Positive-staining cells demonstrate an orange-brown reaction product. Note the presence of F4/80+ 503-PU cells with lobate nuclear morphology of monocytes. (C) An adherent subpopulation 503-PU cells was also positive for the macrophage subset marker sialoadhesin by immunocytochemical staining, whereas no positive cells were found in parental 503 cultures.

Macrophage development can be restored by PU.1 transduction of PU.1-deficient 503 cells. (A) PU.1 transduction of 503 cells (503-PU) restored the development of cells with typical macrophage appearance as shown by Wright-Giemsa staining. (B) Immuno-cytochemistry was used to show that 503-PU cells expressed the macrophage marker F4/80, unlike the parental cells (503). Positive-staining cells demonstrate an orange-brown reaction product. Note the presence of F4/80+ 503-PU cells with lobate nuclear morphology of monocytes. (C) An adherent subpopulation 503-PU cells was also positive for the macrophage subset marker sialoadhesin by immunocytochemical staining, whereas no positive cells were found in parental 503 cultures.

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