, 2004). Thus, this agent binds only in metabolically active mitochondria, resulting in a fluorescent emission. After irradiation, the culture medium was removed and adherent cells were trypsinized. Melanoma cells and melanocytes were pelleted by centrifugation at 1800 rpm for 10 min and resuspended in 5 μL Rhodamine 123 (5 mg/mL) for 30 min at 37 °C. The cells were then washed with phosphate-buffered saline (PBS) and resuspended in FACS flow buffer (Becton

Dickinson). The samples were analyzed for fluorescence (FL-1H detector) on a Becton Dickinson FACScan flow cytometer using Cell Quest software. This experiment was performed 6 h after thermal neutron irradiation. The type D cyclins (with their partner CDKs) form a regulatory selleck kinase inhibitor unit of the G1/S transition that is frequently impaired in neoplásicas (Li et al., 2006). After irradiation, the culture

medium was removed and adherent cells were trypsinized. Melanoma cells and melanocytes were Mitomycin C in vivo pelleted by centrifugation at 1800 rpm for 10 min and incubated with 1 μg specific Anti-cyclin D1 antibody (Santa Cruz, USA) and 10 μL Triton X-100 (0.1%) for 1 h at 4 °C. The cells were then resuspended in FACS Flow buffer. The samples were analyzed for fluorescence (FL-1H detector) on a Becton Dickinson FACScan flow cytometer using Cell Quest software. This experiment was performed 6 h after thermal neutron irradiation. Annexin V is a small Ca2+-dependent protein with high affinity for phosphatidylserine (PS) Vermes et al., 1995. In normal living cells, PS is located in the inner layer of the cell membrane only, but in

apoptotic cells this phospholipid is translocated buy Y-27632 to the outer leaflet. PS exposure on the surface of cells functions as tags for specific recognition for phagocytosis by macrophages or neighboring cells (Fadok et al., 1992). Annexin V was used to detect apoptosis at an early stage in the cells together with propidium iodide, which binds to DNA in cells that have lost membrane integrity (necrotic or late apoptotic cells). After treatment, the cells in the supernatant and the adherent cells were washed with PBS and binding buffer (10 mM HEPES pH7.5 containing 140 mM NaCl and 2.5 mM CaCl2) and stained with 1 μg annexin V-FITC (Santa Cruz Biotechnology, USA) and 18 μg/mL of propidium iodide (PI) (Sigma–Aldrich Corp.). Each sample was analyzed by flow cytometry using the FL-1 and FL-2 channels to distinguish the apoptotic, necrotic, and viable cell populations. The analysis was performed on a FACSCalibur flow cytometer using the Cell Quest software (FACSCalibur; Becton Dickinson). The caspase-3 inhibitor zDEVD-fmk (Becton Dickinson, USA) was prepared as stock solution in 100% DMSO (100 mM). Final concentration in serum-free medium was 1 mM for zDEVD-fmk. Cells were incubated with caspase inhibitor 1 h before addition of BPA.