Research Article

Recovery and Biodistribution of Ex Vivo Expanded Human Erythroblasts Injected into NOD/SCID/IL2R 𝜸 n u l l mice

Figure 4

At day 4 after transfusion, human EBs are mostly detectable in spleen of NOD/SCID/IL2R 𝛾 n u l l mice. (a) Flow cytometric analysis for human CD235a and CFSE expression of bone marrow and spleen cells from transfused and nontransfused (negative control) NOD/SCID/IL2R 𝛾 n u l l mice. The results are representative of those obtained with 2 mice per group (see Table 2 for further details) and are representative of those observed in three separate experiments. (b) Immunocytochemistry for human CD235a of cells from the spleen of untransfused (top left panel) and transfused (lower panels) mice sacrificed 4 days after the human EBs transfusion, as indicated. Cells from control mice (top left panel) are negative while cultured human EBs (top right panel) are all positive. In transfused mice, human C D 2 3 5 a p o s cells (arrows) represented up to 1 8 . 2 ± 5 . 6 % of total splenic cells. However, they were trapped inside larger C D 2 3 5 a n e g cells, probably macrophages of murine origin. Magnifications 40x and 100x, as indicated.
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