Figure 5
Figure 5. CD150− and CD150+ HSCs exhibit differences in contribution to various hematopoietic compartments 24 weeks after transplantation. (A) A significant decrease in donor-derived whole bone marrow (WBM) and thymus engraftment, measured by flow cytometry, was observed for CD150− SPKLS HSCs compared with CD150+ or whole SPKLS HSCs. No statistical difference was observed for donor-derived peripheral blood and spleen chimerism. (B) All 3 populations of SPKLS cells self-renew to give rise to comparable levels of SPKLS, although CD150− SPKLS generate lower levels of KLS, MP, and CLP compartments as measured by flow cytometry. (C) WBM was examined for the presence of donor-derived CD150+ and CD150− SPKLS within transplant recipients that received CD150+ or CD150− SPKLS cells. Both donor populations were able to produce CD150+ and CD150− SPKLS cells, indicating no clear-cut hierarchy between the CD150+ and CD150− SPKLS cells. In addition, CD150+ SPKLS donor cells exhibited a trend toward generating a higher proportion of CD150+ cells in the recipient SP. This result, although not statistically significant, suggests a preference for the CD150+ SPKLS to preferentially produce CD150+ SPKLS on transplantation. Error bars represent SEM.

CD150− and CD150+ HSCs exhibit differences in contribution to various hematopoietic compartments 24 weeks after transplantation. (A) A significant decrease in donor-derived whole bone marrow (WBM) and thymus engraftment, measured by flow cytometry, was observed for CD150 SPKLS HSCs compared with CD150+ or whole SPKLS HSCs. No statistical difference was observed for donor-derived peripheral blood and spleen chimerism. (B) All 3 populations of SPKLS cells self-renew to give rise to comparable levels of SPKLS, although CD150 SPKLS generate lower levels of KLS, MP, and CLP compartments as measured by flow cytometry. (C) WBM was examined for the presence of donor-derived CD150+ and CD150 SPKLS within transplant recipients that received CD150+ or CD150 SPKLS cells. Both donor populations were able to produce CD150+ and CD150 SPKLS cells, indicating no clear-cut hierarchy between the CD150+ and CD150 SPKLS cells. In addition, CD150+ SPKLS donor cells exhibited a trend toward generating a higher proportion of CD150+ cells in the recipient SP. This result, although not statistically significant, suggests a preference for the CD150+ SPKLS to preferentially produce CD150+ SPKLS on transplantation. Error bars represent SEM.

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