Fig. 5.
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.

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 NK1.1sIgM (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 CD25NK1.1 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.

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