Figure 5.
Transplanted human ALDHhiCD133+Lin- cells differentiate into lymphoid and myeloid progeny in vivo. BM from highly engrafted mice that received transplants of 104 to 105 ALDHhiCD133+Lin- cells was stained with human-specific antibodies for mature hematopoietic lineage markers. (A) Human hematopoietic cells were selected by the expression of human CD45 (R2 = 62.5% ± 10.1%, n = 6) and analyzed for myeloid cell markers CD14 and CD33 (B), B-lymphocyte markers CD20 and CD19 (C), and T-lymphocyte markers CD4 and CD8 (D). Lymphoid and myeloid differentiation was observed after the transplantation of purified ALDHhiCD133+Lin- cells. T-lymphocyte production was not supported in the NOD/SCID β2M-null or NOD/SCID mouse.

Transplanted human ALDHhiCD133+Lin- cells differentiate into lymphoid and myeloid progeny in vivo. BM from highly engrafted mice that received transplants of 104 to 105 ALDHhiCD133+Lin- cells was stained with human-specific antibodies for mature hematopoietic lineage markers. (A) Human hematopoietic cells were selected by the expression of human CD45 (R2 = 62.5% ± 10.1%, n = 6) and analyzed for myeloid cell markers CD14 and CD33 (B), B-lymphocyte markers CD20 and CD19 (C), and T-lymphocyte markers CD4 and CD8 (D). Lymphoid and myeloid differentiation was observed after the transplantation of purified ALDHhiCD133+Lin- cells. T-lymphocyte production was not supported in the NOD/SCID β2M-null or NOD/SCID mouse.

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