Figure 7
Figure 7. The fatal anemia is slightly accelerated by pretreatment of Apcdel/+ recipients with ENU. (A) A model showing that Apcfl/+and Apcdel/+ recipients (CD45.2+) were treated with pIpC at 2 months, ENU at 2.5 months (where indicated), and transplanted 4 weeks post-pIpC treatment with CD45.1/CD45.2 WT BM. (B) Kaplan-Meier survival curve of Apcfl/+ (WT) or Apcdel/+ recipients transplanted with CD45.1/CD45.2 WT BM. Recipients treated with ENU are indicated (dashed line). (C) CBC of untreated and ENU-treated Apcfl/+and Apcdel/+recipient mice. RBC, Hb, and MCV were significantly different for both untreated and ENU-treated Apcdel/+recipient mice compared with Apcfl/+-recipient controls. Monocytosis was significant only for the ENU-treated Apcdel/+ vs Apcfl/+-recipient mice. MO, monocytes.

The fatal anemia is slightly accelerated by pretreatment of Apcdel/+recipients with ENU. (A) A model showing that Apcfl/+and Apcdel/+ recipients (CD45.2+) were treated with pIpC at 2 months, ENU at 2.5 months (where indicated), and transplanted 4 weeks post-pIpC treatment with CD45.1/CD45.2 WT BM. (B) Kaplan-Meier survival curve of Apcfl/+ (WT) or Apcdel/+ recipients transplanted with CD45.1/CD45.2 WT BM. Recipients treated with ENU are indicated (dashed line). (C) CBC of untreated and ENU-treated Apcfl/+and Apcdel/+recipient mice. RBC, Hb, and MCV were significantly different for both untreated and ENU-treated Apcdel/+recipient mice compared with Apcfl/+-recipient controls. Monocytosis was significant only for the ENU-treated Apcdel/+ vs Apcfl/+-recipient mice. MO, monocytes.

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