Data are expressed as the percentage of cells in the hypodiploid region

added and after stabilization of the system, the residual oxygen consumption could be determined. The data were analyzed using the DatLab software provided with the instrument. ATP Assay Intracellular ATP was determined using the CellTiter-Glo cell viability assay kit from Promega. 500,000 cells (RAW 264.7) were seeded per well of a 6-well plate and incubated in control medium, galactose medium or 1 mM glucose medium for 4 and 14 hours, 2-DG medium for 1 and 3 hours, or oligomycin-containing medium for 0.5 or 24 hours prior to assay. Cells were washed twice with ice cold PBS and then scraped in 350 ml ice cold 0.6 M perchloric acid (PCA). PCA extracts were centrifuged for 3 minutes at 4000 rpm and 4uC to pellet all cellular protein. Supernatants were neutralized with 140� 155 ml 2 M KOH/0.2 M KH2PO4, pH 7.5 and diluted 1:10 in water. Per well, 100 ml diluted PCA extract was added to 100 ml CellTiter-Glo reagent and the luminescence intensity per well was measured on a LUMIstar OPTIMA microplate luminometer. The ATP concentration was determined using an ATP standard series. For determination of total cellular protein, pellets were dissolved in 250 ml 1 M NaOH and heated for 30 minutes at 95uC. Protein concentration was then measured in 1:50 diluted NaOH extracts. Cellular Actin Staining RAW 264.7 cells on coverslips were pre-incubated in control or 2-DG medium (3 hours), gluc/gal medium (4 and 24 hours), galactose medium (4 and 24 hours), or oligomycin-containing medium (0.5 and 24 hours) and stimulated with 100 ng/ml LPS overnight or left unstimulated. Medium was removed and cells were immediately fixed in 2% paraformaldehyde in 0.2 M sodium phosphate buffer SB-1317 site pubmed ID:http://www.ncbi.nlm.nih.gov/pubmed/19652729 for 30 minutes. Coverslips were washed twice with PBS and twice