Figure 5.
Figure 5. PU.1 is expressed in functional HSCs with long-term reconstituting potential. (A) Sorting gates for the SP fraction. The vast majority of Lin–Sca-1+c-Kit+CD34– cells possessed the SP profile. (B) RT-PCR analysis of PU.1 mRNA in CD34+ or CD34– SP HSCs. HPRT indicates hypoxanthin phosphoribosyltransferase. (C) Expression of GFP in HSCs and GMPs purified from PU.1GFP/+ mice. The vast majority of Lin–Sca-1+c-Kit+ HSCs and SP HSCs expressed PU.1-GFP irrespective of CD34 expression at the single-cell level. GMPs expressed GFP at a higher level compared with HSCs. (D) Ly5.2+ donor type Gr-1+, CD3+, and B220+ cells were successfully reconstituted in a mouse that received a transplant of a single CD34–PU.1-GFP+ HSC. Multilineage reconstitution has been maintained for more than 20 weeks.

PU.1 is expressed in functional HSCs with long-term reconstituting potential. (A) Sorting gates for the SP fraction. The vast majority of LinSca-1+c-Kit+CD34 cells possessed the SP profile. (B) RT-PCR analysis of PU.1 mRNA in CD34+ or CD34 SP HSCs. HPRT indicates hypoxanthin phosphoribosyltransferase. (C) Expression of GFP in HSCs and GMPs purified from PU.1GFP/+ mice. The vast majority of LinSca-1+c-Kit+ HSCs and SP HSCs expressed PU.1-GFP irrespective of CD34 expression at the single-cell level. GMPs expressed GFP at a higher level compared with HSCs. (D) Ly5.2+ donor type Gr-1+, CD3+, and B220+ cells were successfully reconstituted in a mouse that received a transplant of a single CD34PU.1-GFP+ HSC. Multilineage reconstitution has been maintained for more than 20 weeks.

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