Fig. 3.
Fig. 3. Phenotype of spleen cells from primary FGFR3 transplant recipients. / Single-cell suspensions of spleen were prepared from primary BM transplant recipients 6 weeks after transplantation. Cell populations analyzed by flow cytometry are shown for normal littermate controls not receiving transplants (normal, ■), mice receiving empty vector-transplants (MINV, ░), and mice transplanted with MFINV-WT– (WT, ▧) or MFINV-TD– (TD, ▪) expressing BM. MFINV-TD mice displayed a decrease in both normal B (B220+/IgM+) and T (CD3+) lymphocytes, whereas expansions of immature B (B220+/IgM−) lymphocytes and of CD11b+ cells were evident. Mice receiving MFINV-WT BM displayed the same splenic cell phenotype at 6 weeks after transplantation as controls.

Phenotype of spleen cells from primary FGFR3 transplant recipients.

Single-cell suspensions of spleen were prepared from primary BM transplant recipients 6 weeks after transplantation. Cell populations analyzed by flow cytometry are shown for normal littermate controls not receiving transplants (normal, ■), mice receiving empty vector-transplants (MINV, ░), and mice transplanted with MFINV-WT– (WT, ▧) or MFINV-TD– (TD, ▪) expressing BM. MFINV-TD mice displayed a decrease in both normal B (B220+/IgM+) and T (CD3+) lymphocytes, whereas expansions of immature B (B220+/IgM) lymphocytes and of CD11b+ cells were evident. Mice receiving MFINV-WT BM displayed the same splenic cell phenotype at 6 weeks after transplantation as controls.

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