Fig. 5.
Fig. 5. Detailed flow cytometric analysis of the various hematopoietic lineages in bone marrow and spleen of engrafted NOD/SCID. Plots are from a representative experiment in which animals were transplanted with 15 × 106 CD34+ cells and were analyzed after 6 to 8 weeks. (A) Distribution of B-cell markers CD10 and CD20 on all nucleated cells. (B) Distribution of heavy and light-chain cell-surface immunoglobulin on CD19+ human B cells (mean ± SEM of n = 4 to n = 7). All differences between BM and SPL were highly significant (P < .001). (C) Distribution of HLA-DR and CD33 (circles indicate activated HLA-DR+and resting HLA-DR− granulocytes) among CD45+ cells, (D) expression of CD11b and CD16 on CD45+ cells, and (E) expression of human Glycophorin A (Gly A) on CD45− nucleated and enucleated cells. 40,000 events per analysis were recorded.

Detailed flow cytometric analysis of the various hematopoietic lineages in bone marrow and spleen of engrafted NOD/SCID. Plots are from a representative experiment in which animals were transplanted with 15 × 106 CD34+ cells and were analyzed after 6 to 8 weeks. (A) Distribution of B-cell markers CD10 and CD20 on all nucleated cells. (B) Distribution of heavy and light-chain cell-surface immunoglobulin on CD19+ human B cells (mean ± SEM of n = 4 to n = 7). All differences between BM and SPL were highly significant (P < .001). (C) Distribution of HLA-DR and CD33 (circles indicate activated HLA-DR+and resting HLA-DR granulocytes) among CD45+ cells, (D) expression of CD11b and CD16 on CD45+ cells, and (E) expression of human Glycophorin A (Gly A) on CD45 nucleated and enucleated cells. 40,000 events per analysis were recorded.

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