Fig. 3.
Fig. 3. Serial bone marrow transplantations. / Serial bone marrow transplantations demonstrate a significant defect in HSC competition and self-renewal bySca-1−/− mice. Sca-1+/+BM was able to completely repopulate Sca-1−/− mice in both primary and secondary recipients. However, when Sca-1−/− bone marrow was used to repopulate lethally irradiated Sca-1+/+ mice, endogenous Sca-1+/+ HSCs were able to compete against donor stem cells in the primary repopulations (▨). In secondary transplantations using bone marrow from primary recipients to repopulate lethally irradiated Sca-1+/+ mice (▪), the donor bone marrow could not rescue one-third of the recipients from irradiation-induced anemia. Of the remaining recipients, the Sca-1−/− bone marrow contributed approximately 45% to the recipient bone marrow 4 months following repopulation. Three of 9 secondary recipients died.

Serial bone marrow transplantations.

Serial bone marrow transplantations demonstrate a significant defect in HSC competition and self-renewal bySca-1−/−mice. Sca-1+/+BM was able to completely repopulate Sca-1−/− mice in both primary and secondary recipients. However, when Sca-1−/−bone marrow was used to repopulate lethally irradiated Sca-1+/+mice, endogenous Sca-1+/+HSCs were able to compete against donor stem cells in the primary repopulations (▨). In secondary transplantations using bone marrow from primary recipients to repopulate lethally irradiated Sca-1+/+mice (▪), the donor bone marrow could not rescue one-third of the recipients from irradiation-induced anemia. Of the remaining recipients, the Sca-1−/−bone marrow contributed approximately 45% to the recipient bone marrow 4 months following repopulation. Three of 9 secondary recipients died.

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