The bone marrow cells were placed in duplicate 1 mL semisolid agar cultures in 35 mm Petri dishes using 1 × 105 bone marrow cells per culture for the growth of CFU-GM. The cells were cultured in Dulbecco’s Modified Eagle’s Medium (DMEM, Sigma Chemical Co., St. Louis, MO) containing 20% FCS (fetal calf serum) and 0.3% agar. Colony formation was stimulated by the addition of recombinant murine macrophage–granulocyte colony-stimulating factor (rmGM-CSF-Sigma) at a final concentration Smoothened antagonist of 0.5 ng/mL. The

cultures were incubated for 7 days in a fully humidified atmosphere of 5% CO2 in air, and colony formation (clones >50 cells) was scored at 35× magnification using a dissection microscope (Metcalf, 1984). To evaluate the hematopoietic cell populations, whole BM and LTBMC cells were collected by flushing (1 × 106 cells), fixed and labeled. To the verification of mature cells we used 4 antibodies conjugated with four different

fluorocromes: FL1: anti-Gr1-FITC; FL2: anti B220-PE, FL-3:anti-Mac-1-Cy7/PE and FL4: anti-CD3-APC. To analyze the primitive population we used 2 antibodies that Talazoparib recognize the fraction LSK together with a cocktail of mature lineage: FL2: anti-B220, anti-CD3, anti-Ter-119, anti-CD11b and anti-Gr-1, which were all conjugated with PE; FL3: anti Sca-1-Cy7/PE and FL4: anti-c-kit-APC. The data were collected using a FACSCalibur flow cytometer and analyzed using CellQuest software (BD Biosciences). The antibodies were purchased from BD Biosciences. The mice were bled from the heart under deep halothane anesthesia. Within each experimental group, the blood was pooled, left at 37 °C for 30 min, and the clots were allowed to retract overnight at 4 °C. Following centrifugation, the serum was removed and stored at −20 °C. CSA was determined

by measuring the ability of serum obtained from control and experimental groups to Ponatinib research buy stimulate HP to form CFU-GM (1 × 105 cells) from normal mice. The results were expressed as units of CSA/mL, where 1 unit/mL was defined as the lowest amount of CSA able to induce the formation of colonies (Van Den Engh and Bol, 1975). Marrow cells were aseptically collected from two complete femur shafts after killing the animal by cervical dislocation. The plug of marrow cells was gently extruded into a sterile plastic tube using 1 mL of RPMI 1640 medium (Sigma) injected through the femur and then converted to a dispersed cell suspension in 5 mL of RPMI by gently aspirating the suspension up and down 20 times using a sterile 5 mL pipette. To establish the culture, 1 × 107 pooled femoral bone marrow cells were dispensed into T25 tissue culture flasks containing 10 mL of RPMI 1640 supplemented with 25 mM l-glutamine, 25 mM HEPES, 200 UI/mL penicillin, 100 μg/mL streptomycin, 20% horse serum (Sigma), and 0.1 μM hydrocortisone and incubated at 37 °C in 5% CO2.