Typhimurium SL1344 [56]

in HeLa cells was determined using a cell invasion assay. Briefly, overnight bacterial cultures grown in Luria-Bertani broth (LB) were pelleted, resuspended in 1 mL PBS and diluted in DMEM containing 10% FBS to an MOI of ~1:100. An aliquot (0.5 mL) of the bacterial suspension was added to HeLa cells in a 24-well plate and incubated at 37°C in a 5% CO2 atmosphere for 10 minutes. The wells were then washed 3× with PBS and incubated in DMEM for an additional 20 minutes. The medium was removed and the cells were incubated in fresh DMEM containing 100 μg/mL gentamycin for 1.5 hours. Culture media was replaced with fresh DMEM containing 10 μg/mL gentamycin and either 0.1% DMSO, or 10 μM compound D4, D5, D6 or D7. At 2 and 16 hpi, intracellular bacteria were recovered by lysing HeLa cells in PBS containing 1% Triton X-100 and 0.1% SDS. Lysates were serially diluted, plated on LB plates, this website incubated overnight and colonies subsequently counted. HeLa Cell Viability The effect of compound D7 on HeLa cell viability was determined. Briefly, 10 or

100 μM compound D7, or 0.1% DMSO, with or without cycloheximide in MEM, was added to subconfluent HeLa cells in 6-well plates. At 0, 22, 44 and 66 hours supernatants were harvested and tested for the presence of adenylyl kinase using a cytotoxicity S3I-201 in vitro assay (Lonza ToxiLight® BioAssay, Rockland). The cytotoxicity assay was performed as per the manufacturer’s protocol. Briefly, supernatants from HeLa cell cultures incubated in the presence of compound D7 or DMSO (in MEM containing cycloheximide) were tested for evidence of eukaryotic cell cytotoxicity. Aliquots (5 uL) of each supernatant were mixed with 25 uL of Adenylate Kinase Detection Reagent and samples were incubated at room temperature for 5 minutes. Relative light units (RLUs) were measured using a 20/20 n Single Tube Luminometer from Turner BioSystems (Sunnyvale). Assays were conducted in triplicate for each condition. Cell monolayers were washed with warm PBS. 0.75 mL of trypsin was added to each well, and 0.75 mL of MEM was added after

complete trypsinization (trypsinization was monitored by light microscopy). Each sample was thoroughly resuspended and aliquoted into a plastic cuvette aminophylline and the cell number immediately quantitated by determining the optical density at 800 nM [57] using a spectrophotomer. MEK/ERK Activation To determine whether compound D7 interferes with activation of the MEK/ERK pathway, HeLa cells were exposed to compound D7, DMSO, or the specific MEK inhibitor U0126, activated with EGF and then lysates tested by Western blot for TSA HDAC supplier phosphorylated and total ERK as described [43]. Briefly, subconfluent HeLa cells in 6-well plates were serum-starved for 3.5 hours prior to incubation for 45 min. in either 0.1% DMSO, 10 or 100 μM compound D7 or 10 or 25 μM U0126 in serum-free MEM. Cells were then incubated with 100 ng/mL EGF in serum-free MEM for 2 minutes before being scraped in 0.