Figure 2
Figure 2. In vivo reconstitution of myeloid and lymphoid lineages using marrow cells from WT or FX−/− mice injected into FX−/− and WT recipients, and marrow cells from Fuc-T−/− mice injected into Fuc-T−/− recipients. (A) Schematic representation of the transplantation protocol. (B,C) Analysis of peripheral neutrophils (Gr-1+) and lymphocytes (B220+ and CD3ϵ+), and bone marrow myeloid progenitor cells by FACS 4 months after transplantation. Data are means plus or minus SD. Student t test was performed to compare the neutrophil or lymphocyte numbers in each transplant setting with those of WT to WT. P > .5 unless otherwise indicated. (D) One month after transplantation, WT recipient mice receiving donor cells from WT or FX−/− mice were injected intraperitoneally with BrdU and fed with water containing BrdU for 3 days. The percentage of CMP and GMP cells (Lin−c-kit+Sca-1−IL7R−CD34+; numbers on graphs) in S-G2/M phase of the cell cycle was analyzed by anti-BrdU and 7-amino-actinomycin D.

In vivo reconstitution of myeloid and lymphoid lineages using marrow cells from WT or FX−/− mice injected into FX−/− and WT recipients, and marrow cells from Fuc-T−/− mice injected into Fuc-T−/− recipients. (A) Schematic representation of the transplantation protocol. (B,C) Analysis of peripheral neutrophils (Gr-1+) and lymphocytes (B220+ and CD3ϵ+), and bone marrow myeloid progenitor cells by FACS 4 months after transplantation. Data are means plus or minus SD. Student t test was performed to compare the neutrophil or lymphocyte numbers in each transplant setting with those of WT to WT. P > .5 unless otherwise indicated. (D) One month after transplantation, WT recipient mice receiving donor cells from WT or FX−/− mice were injected intraperitoneally with BrdU and fed with water containing BrdU for 3 days. The percentage of CMP and GMP cells (Linc-kit+Sca-1IL7RCD34+; numbers on graphs) in S-G2/M phase of the cell cycle was analyzed by anti-BrdU and 7-amino-actinomycin D.

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