Figure 5
Figure 5. Efficient differentiation of p100−/− pre–pro-B cells into myeloid cells. (A) Lin−B220+CD19−c-Kitlow pre–pro-B cells were sorted from bone marrow of 18- to 20-day-old wild-type and p100−/− mice and cultured as described in “Methods.” After 14 days, cells were collected, stained for CD19 and Mac-1 expression, and analyzed by flow cytometry. Numbers represent mean values (± SD) from 3 mice. (B) Efficient uptake of E coli-FITC bioparticles by in vitro–differentiated Mac-1+ p100−/− myeloid cells. Cultured p100−/− B220+CD19− pre-pro-B cells were incubated after 14 d with FITC-labeled E coli and uptake by CD19+ (----) or Mac-1+ cells (—) was measured by flow cytometry.

Efficient differentiation of p100−/− pre–pro-B cells into myeloid cells. (A) LinB220+CD19c-Kitlow pre–pro-B cells were sorted from bone marrow of 18- to 20-day-old wild-type and p100−/− mice and cultured as described in “Methods.” After 14 days, cells were collected, stained for CD19 and Mac-1 expression, and analyzed by flow cytometry. Numbers represent mean values (± SD) from 3 mice. (B) Efficient uptake of E coli-FITC bioparticles by in vitro–differentiated Mac-1+p100−/− myeloid cells. Cultured p100−/− B220+CD19 pre-pro-B cells were incubated after 14 d with FITC-labeled E coli and uptake by CD19+ (----) or Mac-1+ cells (—) was measured by flow cytometry.

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