Figure 1.
Figure 1. Engraftment of either Atm-/- or Atm+/+ donor bone marrow in conditioned recipients results in stable multilineage chimerism. Lethally irradiated C3H mice were reconstituted with 107 bone marrow cells from either Atm-/- (solid line; n = 6) mutant mice or wild-type littermate controls (dashed line; n = 6). Six weeks after BMT, PBMCs were stained with donor-specific anti-H-2Kb antibodies and analyzed by flow cytometry. Twenty-two weeks after transplantation, blood cells were stained with donor-specific anti-H-2Kb and lineage-specific antibodies and were analyzed by flow cytometry for the presence of donor-derived CD3+, B220+,or CD11b+ after gating. In all experiments, PBMCs from untreated C3H mice were used as negative controls (dotted line).

Engraftment of either Atm-/- or Atm+/+ donor bone marrow in conditioned recipients results in stable multilineage chimerism. Lethally irradiated C3H mice were reconstituted with 107 bone marrow cells from either Atm-/- (solid line; n = 6) mutant mice or wild-type littermate controls (dashed line; n = 6). Six weeks after BMT, PBMCs were stained with donor-specific anti-H-2Kb antibodies and analyzed by flow cytometry. Twenty-two weeks after transplantation, blood cells were stained with donor-specific anti-H-2Kb and lineage-specific antibodies and were analyzed by flow cytometry for the presence of donor-derived CD3+, B220+,or CD11b+ after gating. In all experiments, PBMCs from untreated C3H mice were used as negative controls (dotted line).

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