Fig. 2.
Fig. 2. Multilineage repopulation capacity of transduced and expanded SRCs in primary and secondary mice. / (A) Isotype controls. (B) FACS analysis of BM marrow cells from a primary mouse that had received a transplant 8 weeks previously of 2 × 105 transduced CB CD34+ cells expanded for 4 weeks with FL, TPO, SCF, and IL6. BM cells were analyzed as described in “Materials and methods.” Analysis of lineage markers (CD45/CD19, CD45/CD41, CD45/CD34, CD45/CD14) was performed on cells comprised within the human CD45 gate; analysis of GpA+cells was performed on total BM cells. The numbers in the top right quadrants show the percentages of GFP+ cells within the CD45+ population or within CD34+, CD19+, CD14+, CD41+, and GpA+ cells. (C) Representative FACS profiles of marrow cells from an individual NOD/SCID mouse that had received a transplant 8 weeks previously of unfractionated BM cells of a primary mouse injected with transduced and expanded CB CD34+ cells. GFP positivity and multilineage engraftment were evaluated as described for panel A.

Multilineage repopulation capacity of transduced and expanded SRCs in primary and secondary mice.

(A) Isotype controls. (B) FACS analysis of BM marrow cells from a primary mouse that had received a transplant 8 weeks previously of 2 × 105 transduced CB CD34+ cells expanded for 4 weeks with FL, TPO, SCF, and IL6. BM cells were analyzed as described in “Materials and methods.” Analysis of lineage markers (CD45/CD19, CD45/CD41, CD45/CD34, CD45/CD14) was performed on cells comprised within the human CD45 gate; analysis of GpA+cells was performed on total BM cells. The numbers in the top right quadrants show the percentages of GFP+ cells within the CD45+ population or within CD34+, CD19+, CD14+, CD41+, and GpA+ cells. (C) Representative FACS profiles of marrow cells from an individual NOD/SCID mouse that had received a transplant 8 weeks previously of unfractionated BM cells of a primary mouse injected with transduced and expanded CB CD34+ cells. GFP positivity and multilineage engraftment were evaluated as described for panel A.

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