Figure 1
Figure 1. Human STRC-M and STRC-ML efficiently engraft in IL2RG−/− mice. (A) Representative fluorescence-activated cell sorter profiles of human hematopoietic lineages in BM of IL2RG−/− mouse at 3, 8, and 12 weeks after transplantation of 2 × 105 CD34+ cells. Percentages in fluorescence-activated cell sorter plots refer to lineage marker-positive cells of 2 × 104 total BM cells analyzed. (B) Human CD34+ CB cells show similar multilineage differentiation patterns in the BM of IL2RG−/− mice (n = 10) and B2m−/− mice (n = 10) 3, 8, and 12 weeks after transplantation. (C) In IL2RG−/− mice (n = 12), a larger proportion of CD34+ and GlycA+ cells were detected at 3 weeks and CD33+ cells at 8 weeks after transplantation of human mPB CD34+ cells compared with B2m−/− mice (n = 6). GlycA indicates glycophorin-A; w, weeks; PE, phycoerythrin; and FITC, fluorescein isothiocyanate. Error bars represent SD. *Significant difference (P < .05).

Human STRC-M and STRC-ML efficiently engraft in IL2RG−/− mice. (A) Representative fluorescence-activated cell sorter profiles of human hematopoietic lineages in BM of IL2RG−/− mouse at 3, 8, and 12 weeks after transplantation of 2 × 105 CD34+ cells. Percentages in fluorescence-activated cell sorter plots refer to lineage marker-positive cells of 2 × 104 total BM cells analyzed. (B) Human CD34+ CB cells show similar multilineage differentiation patterns in the BM of IL2RG−/− mice (n = 10) and B2m−/− mice (n = 10) 3, 8, and 12 weeks after transplantation. (C) In IL2RG−/− mice (n = 12), a larger proportion of CD34+ and GlycA+ cells were detected at 3 weeks and CD33+ cells at 8 weeks after transplantation of human mPB CD34+ cells compared with B2m−/− mice (n = 6). GlycA indicates glycophorin-A; w, weeks; PE, phycoerythrin; and FITC, fluorescein isothiocyanate. Error bars represent SD. *Significant difference (P < .05).

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