Figure 5
Figure 5. AMD3100 does not mobilize APL cells from the peritoneal cavity. (A) Kinetics of APL progression following intraperitoneal administration of APL cells. Syngeneic B6129F1 recipient mice (n = 10) were injected intraperitoneally with 106 APL cells and the percentage of Gr-1+CD34+ APL cells in the peritoneum, peripheral blood, spleen, and BM was determined weekly by flow cytometry. APL cells expanded into the peritoneal cavity during the first 2 weeks followed by engraftment in the BM and spleen during the third and fourth weeks. (B,C) Fifteen (B) or 22 (C) days after APL injection, leukemic mice were treated with a single subcutaneous dose of 5 mg/kg AMD3100 and killed 3 hours later. Baseline peritoneum and peripheral blood samples were collected immediately before (pre-AMD) administration of AMD3100. AMD3100-mobilized APL cells into the peripheral blood (B) during the fourth week, but not from the peritoneal cavity (A) during the second week.

AMD3100 does not mobilize APL cells from the peritoneal cavity. (A) Kinetics of APL progression following intraperitoneal administration of APL cells. Syngeneic B6129F1 recipient mice (n = 10) were injected intraperitoneally with 106 APL cells and the percentage of Gr-1+CD34+ APL cells in the peritoneum, peripheral blood, spleen, and BM was determined weekly by flow cytometry. APL cells expanded into the peritoneal cavity during the first 2 weeks followed by engraftment in the BM and spleen during the third and fourth weeks. (B,C) Fifteen (B) or 22 (C) days after APL injection, leukemic mice were treated with a single subcutaneous dose of 5 mg/kg AMD3100 and killed 3 hours later. Baseline peritoneum and peripheral blood samples were collected immediately before (pre-AMD) administration of AMD3100. AMD3100-mobilized APL cells into the peripheral blood (B) during the fourth week, but not from the peritoneal cavity (A) during the second week.

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