Figure 3
Figure 3. Enhanced engraftment by sunitinib is transferable to secondary recipients. CD45.1−CD45.2+ Rag1−/− recipients received sunitinib or vehicle as described in Figure 1A, followed by transfer of 3.3 × 104 electronically sorted HSCs from CD45.1+CD45.2− C57Bl/6 mice on day 0. (A) Sunitinib recipients showed an increased percentage of donor-derived Gr-1 peripheral blood cells compared with vehicle recipients on day 25; N = 4 mice/group. (B) Sixty days after BMT, whole BM from recipients described in panel A was transferred to lethally irradiated CD45.1−CD45.2+ C57Bl/6 mice. (C) Frequencies of CD45.1+ cells in the recipients of the secondary transplantation are shown 7 months after the secondary transplantation: n = 8 for sunitinib group; n = 5 for vehicle group. Similar results were seen on day 32 and day 63 after the secondary transplantation. *P < .05. **P < .001.

Enhanced engraftment by sunitinib is transferable to secondary recipients. CD45.1CD45.2+Rag1−/− recipients received sunitinib or vehicle as described in Figure 1A, followed by transfer of 3.3 × 104 electronically sorted HSCs from CD45.1+CD45.2 C57Bl/6 mice on day 0. (A) Sunitinib recipients showed an increased percentage of donor-derived Gr-1 peripheral blood cells compared with vehicle recipients on day 25; N = 4 mice/group. (B) Sixty days after BMT, whole BM from recipients described in panel A was transferred to lethally irradiated CD45.1CD45.2+ C57Bl/6 mice. (C) Frequencies of CD45.1+ cells in the recipients of the secondary transplantation are shown 7 months after the secondary transplantation: n = 8 for sunitinib group; n = 5 for vehicle group. Similar results were seen on day 32 and day 63 after the secondary transplantation. *P < .05. **P < .001.

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