Fig. 4.
Fig. 4. Thymic repopulation by cultured CD34+CD38−Lin− cells in vivo. Flow cytometric analysis of SCID-hu thymocytes, 30 days after injection with transduced CD34+CD38−Lin− cells, precultured for 3 weeks in TPO + FL + SCF. (A) Dot plot shows anti-HLA–A3 FITC staining plus GFP fluorescence versus CD3 APC staining. (B) Dot plot shows GFP fluorescence versus CD3 APC staining; cells were not stained with anti–HLA-A3 FITC. (C) Dot plots show CD4 APC versus CD8β and CD4 APC versus CD3 PE staining for cells stained with anti–HLA-A3 FITC as in (A), gated on either FITC−GFP− cells (acceptor cells) or FITC+GFP+ cells (donor cells); and for cells not stained with anti-HLA–A3 FITC as in (B), gated on GFP+ cells (transduced GFP+ donor cells). Quadrants were set to include 99% of cells stained with isotypic control and GFP− cells in lower left quadrants. Data shown are representative of 2 independent experiments with 2 different donors.

Thymic repopulation by cultured CD34+CD38Lin cells in vivo. Flow cytometric analysis of SCID-hu thymocytes, 30 days after injection with transduced CD34+CD38Lin cells, precultured for 3 weeks in TPO + FL + SCF. (A) Dot plot shows anti-HLA–A3 FITC staining plus GFP fluorescence versus CD3 APC staining. (B) Dot plot shows GFP fluorescence versus CD3 APC staining; cells were not stained with anti–HLA-A3 FITC. (C) Dot plots show CD4 APC versus CD8β and CD4 APC versus CD3 PE staining for cells stained with anti–HLA-A3 FITC as in (A), gated on either FITCGFP cells (acceptor cells) or FITC+GFP+ cells (donor cells); and for cells not stained with anti-HLA–A3 FITC as in (B), gated on GFP+ cells (transduced GFP+ donor cells). Quadrants were set to include 99% of cells stained with isotypic control and GFP cells in lower left quadrants. Data shown are representative of 2 independent experiments with 2 different donors.

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