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4 protocols using rpmi 1640

1

Synthesis and Cytotoxicity of 3-N-Alkyloxyestradiol

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The 3-N-alkyloxyestradiol derivative, 3-[2-diisopro-pylamino]-ethoxy-D1,3,5 (10)-estrien-17-one (DI) was synthesized and provided by Dr. John Cooperwood (Florida A&M University, Tallahassee, FL, USA). Propidium iodide, DMSO (dimethyl sulfoxide), D-Glucose and Ethanol was obtained from Sigma-Aldrich (St. Louis, MO, USA). RPMI 1640, penicillin-streptomycin antibiotic solution (10,000 UI/mL), 0.25% Trypsin-EDTA solution and phosphate buffer (PBS) were all obtained from Invitrogen/Life Technologies (Carlsbad, California, USA). fetal bovine serum (FBS) was obtained from Atlanta Biologicals (Flowery Branch, GA, USA). Quick Start Bradford Reagent, 1X (BioRad, Hercules, CA) and Ready 2-D Starter Kit were obtained from BioRad (Hercules, CA, USA).
PC-3 cells were cultured in RPMI 1640 medium supplemented with 10% fetal bovine serum and penicillin-streptomycin antibiotic solution (10,000 UI/mL), at 37°C in a 5% CO2 humidified atmosphere. A stock solution was prepared by dissolving 3-[2-diisopropylamino]-ethoxy-D1,3,5(10)-estrien-17-one (DI) in 100% DMSO (Sigma-Aldrich) with subsequent dilutions made in cell culture medium. In our experimental conditions, PC-3 cells were treated for 48 h with DI. Cells were detached with 0.25% Trypsin-EDTA solution washed and collected.
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2

Cell Culture Protocols for L929 and AGS

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Iran’s National Cell Bank (NCBI, Tehran, Iran) was the source for purchasing L929 and AGS cell lines. The culturing of the cells happened in the medium of RPMI-1640 accompanied by 100 μg/ml streptomycin, 100 IU/ml penicillin, 10% fetal bovine serum inactivated by heat (Bio-Rad, San Diego, CA, USA) at 37ºC and moisturized atmosphere, with 5% CO2 - 95% O2. When the cultured cells reached the suitable confluence, they got subjected to passage (Karimabad et al., 2017a; Karimabad et al., 2017b).
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3

Isolation and characterization of MSC-derived EVs

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The MSCs were supplied by Lonza (Lonza, Basel, Switzerland) and cultured in the presence of MSC basal medium (MSCBM; Lonza). MSC-derived EVs were collected from the supernatant of MSCs cultured overnight in RPMI-1640 (Lonza) supplemented with 0.5% of BSA (Sigma-Aldrich, St. Louis, MO, USA). The cell supernatant was centrifuged twice at 3,000 × g for 20 min to remove cell debris and then ultracentrifuged at 100,000 × g (Beckman Coulter Optima L-90K ultracentrifuge; Beckman Coulter, Brea, CA, USA) for 1 h at 4ºC. EVs were stored in serum-free RPMI-1640 supplement with 1% DMSO at −80ºC. EV protein content was quantified by the Bradford method (Bio-Rad, Hercules, CA, USA).
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4

Culturing Murine Hepatocellular Carcinoma Cells

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Murine HCC Hepa1-6 cells (American Type Culture Collection) were cultured in Dulbecco's modified Eagle's medium, and murine HCC H22 cells, (Bio-Rad Laboratories, Inc.) in RPMI 1640 at 37°C (5% CO2) in a humidified incubator. The media contained 10% fetal bovine serum, 100 U/ml penicillin and 100 µg/ml streptomycin. All other reagents were purchased from Thermo Fisher Scientific, Inc., unless otherwise stated.
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