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4 protocols using dme h 21

1

Placental Explants Exposure to mRNA Vaccines

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Placental biopsies were washed in Cytowash (consisting of DME/H-21 (Gibco), 2.5% fetal bovine serum (Hyclone), 1% glutamine plus (Atlanta Biologicals), 1% penicillin/streptomycin (Invitrogen), and 1% gentamicin (Gibco) 38 (link) and dissected into 1.0 cm2 chorionic villi explants. A single villus was placed in one well of a 24-well plate containing 0.5 ml of prewarmed cell free media [DME/H-21, 2% Nutridoma (Roche), 1% sodium pyruvate (Sigma), 1% Hepes buffer (Invitrogen), 1% glutamate plus (Atlanta Biologicals), and 1% penicillin/streptomycin (Invitrogen)] with 10% fetal bovine serum and incubated at 37°C in 5% CO2/95% for 30 minutes. Vaccine mixtures for explant exposure were then prepared such that final vaccine concentrations were: BNT162b2 and mRNA-1273 vaccine 0.1 μg/mL and 1 μg/mL, as well as control medium. Testing concentrations were based on estimates of localized circulating levels of mRNA vaccines in organs of mice vaccinated for influenza 28 (link). Explants were exposed for 0.5 or 4 hours and incubated at 37°, after which 200 ul of supernatant were collected and stored at −4°C for cytokine analysis. Exposed explants were washed in PBS and then stored at −80 °C until RNA extraction, or formalin-fixed for 24 hours at room temperature, then washed in 70% ethanol and stored at −4°C until undergoing paraffin embedding.
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2

Placental Explant Exposure to mRNA Vaccines

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Placental biopsies were washed in Cytowash (consisting of DME/H-21 (Gibco), 2.5% fetal bovine serum (HyClone), 1% glutamine plus (Atlanta Biologicals, Minneapolis, MN), 1% penicillin/streptomycin (Invitrogen), and 1% gentamicin (Gibco)42 (link) and dissected into 1.0 cm2 chorionic villi explants. A single villus was placed in one well of a 24-well plate containing 0.5 mL of prewarmed cell free media [DME/H-21, 2% Nutridoma (Roche, Basel, Switzerland), 1% sodium pyruvate (Sigma-Aldrich, St. Louis, MO), 1% HEPES buffer (Invitrogen), 1% glutamate plus (Atlanta Biologicals), and 1% penicillin/streptomycin (Invitrogen)] with 10% fetal bovine serum and incubated at 37°C in 5% CO2/95% O2 for 30 min. Vaccine mixtures for explant exposure were then prepared such that final vaccine concentrations were: BNT162b2 and mRNA-1273 vaccine 0.1 μg/mL and 1 μg/mL, as well as control medium. Testing concentrations were based on estimates of localized circulating levels of mRNA vaccines in organs of mice vaccinated for influenza.28 (link) Explants were exposed for 0.5 or 4 h and incubated at 37°C, after which 200 μl of supernatant were collected and stored at -4°C for cytokine analysis. Exposed explants were washed in PBS and then stored at −80°C until RNA extraction, or formalin-fixed for 24 h at room temperature, then washed in 70% ethanol and stored at -4°C until undergoing paraffin embedding.
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Cultivation of Human Brain Cell Lines

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Normal human brain astroglia cell line SVG p12 (CRL-8621) was obtained from ATCC (Manassas, VA, USA) and cultured in EMEM (Gibco, Waltham, MA, USA). Normal human astrocyte (HA; Catalog #1800) was obtained from ScienCell (Carlsbad, CA, USA) and cultured in Astrocyte medium (AM; Catalog #1801, ScienCell). Glioma cell line U87 (HTB-14) was obtained from ATCC and cultured in EMEM (Gibco). Glioma cell line SHG-44 (3131C0001000700048) was obtained from Cell Resource Center, Shanghai Institute of Life Sciences, Chinese Academy of Sciences (Shanghai, China) and cultured in RPMI 1640 (w/o Hepes; Gibco). Glioma cell line GOS-3 (ACC 408) was obtained from German Collection of Microorganisms and Cell Cultures (Braunschweig, Germany) and cultured in Dulbecco’s MEM (Gibco). Glioma cell line TJ905 (3111C0001CCC000267) was obtained from Cell Resource Center, Shanghai Institute of Life Sciences, Chinese Academy of Sciences and cultured in DMEM-H: Dulbecco’s modified Eagle’s medium (DME H-21 4.5 g/Liter Glucose; Gibco). All glioma cell lines were cultured in medium supplemented with 10% FBS (Invitrogen, Waltham, MA, USA). All cells were cultured at 37 °C in 5% CO2.
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Placental Tissue Collection Protocol

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All methods were approved by the UCSF Institutional Review Board. Informed consent was obtained from all donors. Second trimester placentas were collected following elective terminations and placed in cytowash medium [DME/H-21 (Gibco), 12.5% fetal bovine serum (Hyclone), 1% glutamine plus (Atlanta Biologicals), 1% penicillin/streptomycin (Invitrogen) and 0.1% gentamicin (Gibco)]. Tissue samples were stored on ice prior to dissection.
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