Figure 1
Figure 1. WS1.6 promoter results in limited selection of WASp+ cells in vivo. (A) Experimental design for in vivo promoter comparison studies. WASp−/− congenically marked HSC were transduced with either MND or WS1.6-containing LV and cotransplanted into lethally irradiated WASp−/− CD45.1+CD45.2+ recipients. (B) WASp expression in peripheral blood mononuclear subsets was examined by intracellular staining at different time points; monocytes (CD11b+GR1low); B cells (B220+CD3−); and T cells (B220−CD3+). (C) Viral copy numbers in sorted CD45.1+ or CD45.2+ BM CD11b+ monocytes were analyzed by qPCR. (D) Representative WASp staining in splenic T-and B-cell subsets, with the summary WASp expression data shown for T cells (E) and for B cells (F). To quantify WASp expression in different subsets, we analyzed MFI of WASp+ cells within the T- (G) and B-cell (H) lineages. Data represent 2 unique experiments with error bars showing standard deviation (SD), n = 8 for MND and 7 for WS1.6 (*P < .05; **P < .01; ***P < .001).

WS1.6 promoter results in limited selection of WASp+ cells in vivo. (A) Experimental design for in vivo promoter comparison studies. WASp−/− congenically marked HSC were transduced with either MND or WS1.6-containing LV and cotransplanted into lethally irradiated WASp−/− CD45.1+CD45.2+ recipients. (B) WASp expression in peripheral blood mononuclear subsets was examined by intracellular staining at different time points; monocytes (CD11b+GR1low); B cells (B220+CD3); and T cells (B220CD3+). (C) Viral copy numbers in sorted CD45.1+ or CD45.2+ BM CD11b+ monocytes were analyzed by qPCR. (D) Representative WASp staining in splenic T-and B-cell subsets, with the summary WASp expression data shown for T cells (E) and for B cells (F). To quantify WASp expression in different subsets, we analyzed MFI of WASp+ cells within the T- (G) and B-cell (H) lineages. Data represent 2 unique experiments with error bars showing standard deviation (SD), n = 8 for MND and 7 for WS1.6 (*P < .05; **P < .01; ***P < .001).

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