Fig. 3.
Fig. 3. Flow cytometry of day 19 fetal livers showing separation of B-lineage subsets in Eμ-ret (Tg+) and transgene-negative (Tg−) mice. In the upper diagrams, B-lineage cells (CD45R+) are resolved from total liver cells into less differentiated (CD43+) and more differentiated subsets (CD43−). The percentages of CD45R+CD43− (left upper quadrant) and CD45R+CD43+ (right upper quadrant) cells among total liver cells are shown in the corresponding quadrant. In the lower diagrams, CD45R+CD43+ cells are further resolved into BP-1− early pro-B (bottom region), CD24+BP-1+ late pro-B (upper left region), and CD24++ BP-1+ early pre-B cells (upper right region) and their percentages are shown in their corresponding region. An arrow points to a population of late pro-B cells that expresses high levels of BP-1, as previously observed in the bone marrow of 3-to 5-week-old Eμ-ret mice.

Flow cytometry of day 19 fetal livers showing separation of B-lineage subsets in Eμ-ret (Tg+) and transgene-negative (Tg−) mice. In the upper diagrams, B-lineage cells (CD45R+) are resolved from total liver cells into less differentiated (CD43+) and more differentiated subsets (CD43). The percentages of CD45R+CD43 (left upper quadrant) and CD45R+CD43+ (right upper quadrant) cells among total liver cells are shown in the corresponding quadrant. In the lower diagrams, CD45R+CD43+ cells are further resolved into BP-1 early pro-B (bottom region), CD24+BP-1+ late pro-B (upper left region), and CD24++ BP-1+ early pre-B cells (upper right region) and their percentages are shown in their corresponding region. An arrow points to a population of late pro-B cells that expresses high levels of BP-1, as previously observed in the bone marrow of 3-to 5-week-old Eμ-ret mice.

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