Fig. 5.
The majority of early CD45R+ pro-B cells in BM are c-kit−. The boxed region of Panel A shows CD45R+CD43+ cells in lymphoid-enriched BM, from which BP-1− CD25− NK1.1−sIgM− (B) cells were sorted. These gating criteria allowed isolation of early CD45R+ pro-B cells that were subsequently stained for surface c-kit, fixed, permeabilized, and stained for intranuclear TdT. Expression of c-kit (C) and TdT (D) in this costained population is shown. Panel E shows c-kit expression in the gated TdT+ cells within CD45R+CD43+ BP-1− CD25−NK1.1− sIgM− cells. The frequencies of these subsets in BM are shown in Table 3. Means are from two independent experiments performed on pooled marrow from five or seven mice.