Figure 4
Figure 4. Thymic granulocyte development is IL-7Rα dependent. (A) The development of CD45.2+ ETPs and thymic granulocytes in the absence of IL-7Rα was examined in competitive BM chimeras 8 weeks after reconstitution of lethally irradiated CD45.1+ hosts. (B) The development of CD45.2+ BM Lin−Sca1+Kit+ (LSK) and splenic granulocytes in the absence of IL-7Rα was examined in mixed BM chimeras 8 weeks after reconstitution of lethally irradiated CD45.1+ hosts. (C) Shown is the mean percent CD45.2+ donor contribution to BM LSK, splenic granulocytes, ETPs, or thymic granulocytes by IL-7Rα+/+ (black bars) or IL-7Rα−/− (gray bars) BM. Three mice per group were examined. Error bars represent SEM. ***P < .001 for the CD45.2+ donor chimerism of the indicated population compared with BM LSK CD45.2+ donor chimerism.

Thymic granulocyte development is IL-7Rαdependent. (A) The development of CD45.2+ ETPs and thymic granulocytes in the absence of IL-7Rα was examined in competitive BM chimeras 8 weeks after reconstitution of lethally irradiated CD45.1+ hosts. (B) The development of CD45.2+ BM LinSca1+Kit+ (LSK) and splenic granulocytes in the absence of IL-7Rα was examined in mixed BM chimeras 8 weeks after reconstitution of lethally irradiated CD45.1+ hosts. (C) Shown is the mean percent CD45.2+ donor contribution to BM LSK, splenic granulocytes, ETPs, or thymic granulocytes by IL-7Rα+/+ (black bars) or IL-7Rα−/− (gray bars) BM. Three mice per group were examined. Error bars represent SEM. ***P < .001 for the CD45.2+ donor chimerism of the indicated population compared with BM LSK CD45.2+ donor chimerism.

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