The uptake levels of FSL-1 by the cells were analysed by using FCM as described above and assessed by change AZD6738 price in the mean fluorescence intensity (MFI). For an assay using a confocal laser scanning microscope (CLSM, LSM510 invert Laser Scan Microscope, Carl Zeiss,

Tokyo, Japan), a 2-ml suspension of the cells (1 × 105/ml) was added to each well of a six-well plate and incubated at 37° for 24 hr. Then the cells were washed three times at 37° with appropriate base medium and incubated with FITC-FSL-1. The cells were washed with PBS and reacted for 20 min with 50 μg/ml Alexa-Con A in PBS and then treated with PBS containing 3% (w/v) paraformaldehyde. To exclude non-specific incorporation of FSL-1, inhibition of FITC-FSL-1 uptake by unlabelled FSL-1 was also examined. Uptake of FITC-FSL-1 was measured in the presence of 9 or 35 μg/ml unlabelled FSL-1 under the experimental conditions described www.selleckchem.com/products/17-AAG(Geldanamycin).html above. To test the effects of Nys, CPZ and MbCD on FSL-1 uptake, RAW264.7 cells were treated for 30 min with various concentrations of the inhibitors as indicated in Fig. 4, which do not affect the viability of the cells.

After the cells had been washed with RPMI-1640 base medium, the uptake level of FSL-1 was determined as described above. A mouse clathrin heavy-chain-specific small interfering RNA (siRNA) (ACUAAGUAGCGAGAAAGGCtt) and negative control siRNA were purchased from Applied Biosystems (Foster City, CA). A 500-μl suspension of RAW264.7 cells (5 × 105 cells/ml) in a 24-well plate was prepared with antibiotic-free RPMI-1640 complete medium. The cells were incubated for 24 hr and then transfected with the siRNA (20 pmol/well) by using Lipofectamine 2000 according to the manufacturer’s instructions. The medium was exchanged at 5 hr and 24 hr after transfection, and the cells were examined for FSL-1 uptake at 48 hr after transfection. To confirm the effects of siRNAs, Real-Time TaqMan PCR was performed according to the manufacturer’s standard PCR protocol by using a

StepOne Real-Time PCR system (Applied Biosystems) with Rucaparib concentration specific pre-made TaqMan probes for mouse clathrin heavy chain (CGTTAATTGACCAGGTTGTACAGAC, Applied Biosystems) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH; GAACGGATTTGGCCGTATTGGGCGC, Applied Biosystems). For down-regulation of CD14 or CD36, their specific siRNA cocktails were purchased from Santa Cruz Biotechnology (Santa Cruz, CA). Eighty picomoles of siRNA or negative control siRNA were transfected into HEK293/CD14 or HEK293/CD36 using Metafectene (Biontex Laboratories GmbH). The effects of siRNA transfection on CD14 and CD36 expression level were confirmed by FCM analysis. HEK293 cells were prepared in a six-well plate (5 × 105/well). Then the cells were transiently transfected with CD14 (1 or 2 μg) and/or CD36 (1 or 2 μg). After a 48-hr incubation, FITC-FSL-1 (100 μg/ml) was added and the uptake level was determined.