Figure 3.
Figure 3. Evaluation of IFN-γ on primitive and mature myeloid progenitor numbers isolated from the BM of Fanca–/–, Fancg–/–, and Fancc–/– mice. (A) Evaluation of myeloid progenitors from WT, Fancc–/– , Fanca–/–, and Fancg–/– bone marrow. Hematopoietic cells derived from the bone marrow LDMNCs from mice of each respective genotype were cultured in triplicate to evaluate growth of high proliferating potential colony-forming cells (HPP-CFCs) and low proliferating potential colony-forming cells (LPP-CFCs). Data represent the mean ± standard error of the mean (SEM) of 3 independent experiments. (B) Bone marrow cells from WT, Fancc–/–, Fanca–/–, and Fancg–/– mice previously treated with a 7-day course of 400 μg/kg per day IFN-γ or vehicle control were cultured at 2 × 104 BM LDMNCs/mL to determine the reduction in the respective populations of progenitors. Data represent the mean ± standard error of the mean (SEM) of 3 independent experiments.

Evaluation of IFN-γ on primitive and mature myeloid progenitor numbers isolated from the BM of Fanca/, Fancg/, and Fancc/ mice. (A) Evaluation of myeloid progenitors from WT, Fancc/, Fanca/, and Fancg/ bone marrow. Hematopoietic cells derived from the bone marrow LDMNCs from mice of each respective genotype were cultured in triplicate to evaluate growth of high proliferating potential colony-forming cells (HPP-CFCs) and low proliferating potential colony-forming cells (LPP-CFCs). Data represent the mean ± standard error of the mean (SEM) of 3 independent experiments. (B) Bone marrow cells from WT, Fancc/, Fanca/, and Fancg/ mice previously treated with a 7-day course of 400 μg/kg per day IFN-γ or vehicle control were cultured at 2 × 104 BM LDMNCs/mL to determine the reduction in the respective populations of progenitors. Data represent the mean ± standard error of the mean (SEM) of 3 independent experiments.

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