Figure 3.
Figure 3. Purified CCE-25–c-Kitneg cell growth in RAG-2–/– mice. CCE-25–c-KitnegSca-1pos and Sca-1neg cells were purified by elutriation and cell sorting as described in “Materials and methods.” These cells were transplanted into sublethally irradiated RAG-2–/– mice (4.0 Gy). At 14 weeks after transplantation, the thymuses were harvested and assayed for the presence of donor (Ly 5.2) thymocytes (CD3ϵ). Animals received transplants of saline (A), 1 × 106 whole bone marrow (wBMC, positive control) (B), 1 × 103 CCE-25–c-KitnegSca-1pos (C), or 1 × 103 CCE-25–c-KitnegSca-1neg cells (D). These results are representative of 5 animals per group and 2 separate experiments.

Purified CCE-25–c-Kitneg cell growth in RAG-2–/– mice. CCE-25–c-KitnegSca-1pos and Sca-1neg cells were purified by elutriation and cell sorting as described in “Materials and methods.” These cells were transplanted into sublethally irradiated RAG-2–/– mice (4.0 Gy). At 14 weeks after transplantation, the thymuses were harvested and assayed for the presence of donor (Ly 5.2) thymocytes (CD3ϵ). Animals received transplants of saline (A), 1 × 106 whole bone marrow (wBMC, positive control) (B), 1 × 103 CCE-25–c-KitnegSca-1pos (C), or 1 × 103 CCE-25–c-KitnegSca-1neg cells (D). These results are representative of 5 animals per group and 2 separate experiments.

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